| Diseases |
Alias |
|
| Silver-Russell Syndrome 3 |
|
Growth Restriction, Severe, With Distinctive Facies
|
SRS3
|
|
Grdf
|
|
|
| Silver-Russell Syndrome 1 |
|
Silver-Russell Syndrome
|
Russell-Silver Syndrome
|
|
Silver-Russell Dwarfism
|
Rss
|
|
SRS1
|
Srs
|
|
Silver Russell Dwarfism
|
Russell Silver Syndrome
|
|
Silver Russell Syndrome
|
|
|
| Silver-Russell Syndrome Due To A Point Mutation |
|
|
| Hemihyperplasia, Isolated |
|
Hemihypertrophy
|
Hemihyperplasia
|
|
Isolated Hemihyperplasia
|
IH
|
|
Hhp
|
Hemihypertrophy, Isolated
|
|
Hemi 3 Syndrome
|
Hemicorporal Hypertrophy
|
|
Isolated Hemihypertrophy
|
Hemi-3 Syndrome
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Beckwith-Wiedemann Syndrome |
|
Wiedemann-Beckwith Syndrome
|
BWS
|
|
Exomphalos-Macroglossia-Gigantism Syndrome
|
Emg Syndrome
|
|
Beckwith-Wiedemann Syndrome Due To Cdkn1c Mutation
|
Emg Abnormality
|
|
Wbs
|
Exomphalos Macroglossia Gigantism Syndrome
|
|
Beckwith-Wiedemann Syndrome Due To Nsd1 Mutation
|
Macroglossia Exomphalos Gigantism
|
|
|
| Wilms Tumor 1 |
|
Nephroblastoma
|
Wilms Tumor
|
|
WT1
|
Wilms' Tumor
|
|
Bilateral Wilms Tumor
|
Wilms Tumor, Type 1
|
|
Wilms Tumor, Somatic
|
Adult Nephroblastoma
|
|
Wt1 Disorder
|
Renal Embryonic Tumor
|
|
Adult Kidney Wilms Tumor
|
Childhood Kidney Wilms Tumor
|
|
Nonanaplastic Kidney Wilms Tumor
|
|
|
| Adrenal Carcinoma |
|
Adrenal Cancer
|
Adrenal Gland Cancer
|
|
Malignant Neoplasm Of Adrenal Gland
|
Adrenal Gland Neoplasms
|
|
Carcinoma Of The Adrenal Gland
|
Adrenal Neoplasm
|
|
Malignant Adrenal Tumor
|
Neoplasm Of Adrenal Gland
|
|
Tumor Of The Adrenal Gland
|
Adrenal Gland Neoplasm
|
|
Adrenocortical Carcinoma
|
Adrenal Gland Malignancy
|
|
Suprarenal Cancer
|
Malignant Neoplasm Of Suprarenal Gland
|
|
Malignant Neoplasm Of Adrenal Gland, Unspecified
|
Malignant Tumour Of Adrenal Gland
|
|
Suprarenal Gland Cancer
|
Primary Malignant Neoplasm Of Adrenal Gland
|
|
|
| Silver-Russell Syndrome Due To An Imprinting Defect Of 11p15 |
|
|
| Silver-Russell Syndrome Due To 11p15 Microduplication |
|
|
| Beckwith-Wiedemann Syndrome Due To Imprinting Defect Of 11p15 |
|
|
| Acid-Labile Subunit Deficiency |
|
Short Stature Due To Primary Acid-Labile Subunit Deficiency
|
ACLSD
|
|
Acid-Labile Subunit, Deficiency Of
|
Decreased Levels Of Acid Labile Subunit
|
|
Growth Disorders
|
|
|
| Hypoglycemia |
|
Hypoglycaemia
|
Low Blood Sugar
|
|
Hypoglycaemia Nos
|
Spontaneous Hypoglycaemia
|
|
Nondiabetic Hypoglycaemia
|
Hypoglycaemic Disorder Nos
|
|
Hypoglycaemic Syndrome
|
|
|
| Congenital Mesoblastic Nephroma |
|
Mesoblastic Nephroma
|
Nephroma, Mesoblastic
|
|
|
| Hypoglycemic Coma |
|
|
| Fetal Macrosomia |
|
|
| Maturity-Onset Diabetes Of The Young |
|
MODY
|
Maturity Onset Diabetes Mellitus In Young
|
|
Mason-Type Diabetes
|
Mason Type Diabetes
|
|
Maturity Onset Diabetes Of The Young
|
Mody Syndrome
|
|
Diabetes Of The Young, Maturity-Onset
|
|
|
| Potter'S Syndrome |
|
Potter Sequence
|
Potter Syndrome
|
|
Oligohydramnios Sequence
|
Congenital Absence Of Kidneys Syndrome
|
|
|
| Hemangiopericytoma, Malignant |
|
Hemangiopericytoma
|
Haemangiopericytic Meningioma
|
|
Malignant Hemangiopericytoma
|
Solitary Fibrous Tumor
|
|
|
| Secondary Hypertrophic Osteoarthropathy |
|
Osteoarthropathy, Secondary Hypertrophic
|
Bamberger-Marie Disease
|
|
Hpoa - Hypertrophic Pulmonary Osteoarthropathy
|
Hypertrophic Pulmonary Osteoarthropathy
|
|
Marie Bamberger Disease
|
|
|
| Rhabdomyosarcoma |
|
|
| Laron Syndrome |
|
Growth Hormone Insensitivity Syndrome
|
Growth Hormone Receptor Deficiency
|
|
Laron Dwarfism
|
Pituitary Dwarfism Ii
|
|
Laron-Type Isolated Somatotropin Defect
|
Primary Growth Hormone Resistance
|
|
Laron-Type Dwarfism
|
Laron Type Pituitary Dwarfism I
|
|
Primary Growth Hormone Insensitivity
|
Primary Gh Resistance
|
|
Gh-R Deficiency
|
Growth Hormone Receptor Defect
|
|
Laron-Type Pituitary Dwarfism
|
Laron-Type Short Stature
|
|
Severe Gh Insensitivity
|
Ghis
|
|
Short Stature Due To A Defect In Growth Hormone Receptor Or Post-Receptor Pathway
|
Complete Growth Hormone Insensitivity
|
|
Gh Receptor Deficiency
|
Primary Gh Insensitivity
|
|
Short Stature Due To Growth Hormone Resistance
|
LARS
|
|
|
| Papilloma |
|
|
| Acromegaly |
|
Gigantism
|
Growth Hormone Excess
|
|
Pituitary Giant
|
Somatotroph Adenoma
|
|
Growth Hormone-Secreting Pituitary Adenoma
|
|
|
| Liver Fibroma |
|
Fibroma Of The Liver
|
Liver Solitary Fibrous Tumor
|
|
|
| Hepatoblastoma |
|
|
| Polycystic Ovary Syndrome |
|
Polycystic Ovarian Syndrome
|
Pcos
|
|
Polycystic Ovarian Disease
|
Polycystic Ovaries
|
|
Stein-Leventhal Syndrome
|
Multicystic Ovaries
|
|
Polycystic Ovary
|
Sclerocystic Ovaries
|
|
Sclerocystic Ovary Syndrome
|
Stein-Leventhal Synd.
|
|
Cystic Disease Of Ovaries
|
Cystic Disease Of Ovary
|
|
Pco
|
Pcod
|
|
Sclerocystic Ovarian Degeneration
|
Polycystic Ovary Syndrome, Susceptibility To
|
|
Pcos - [Polycystic Ovary Syndrome]
|
Polycystic Ovary Nos
|
|
Pco - [Polycystic Ovary]
|
|
|
| Retroperitoneal Hemangiopericytoma |
|
|
| Nephroma |
|
|
| Insulin-Like Growth Factor I |
|
Insulin-Like Growth Factor I Deficiency
|
IGF1 DEFICIENCY
|
|
Insulin-Like Growth Factor I, Resistance To
|
Growth Retardation With Deafness And Mental Retardation Due To Igf1 Deficiency
|
|
Growth Delay Due To Insulin-Like Growth Factor Type 1 Deficiency
|
Growth Delay Due To Insulin-Like Growth Factor I Resistance
|
|
IGF1RES
|
Igf-I Resistance
|
|
Somatomedin, End-Organ Insensitivity To
|
Somatomedin-C
|
|
Somatomedin-C, Resistance To
|
Growth Retardation With Sensorineural Deafness And Mental Retardation
|
|
Insulin-Like Growth Factor 1 Resistance To
|
Igf-1 Resistance
|
|
Somatomedin End-Organ Insensitivity To
|
Somatomedin-C Resistance To
|
|
Growth Restriction With Sensorineural Deafness And Intellectual Disability
|
Growth Delay-Deafness-Intellectual Disability Syndrome
|
|
Growth Delay-Hearing Loss-Intellectual Disability Syndrome
|
Igf-1 Deficiency
|
|
Primary Insulin-Like Growth Factor Deficiency
|
Resistance To Igf-1
|
|
Insulin-Like Growth Factor 1 Resistance
|
End-Organ Insensitivity To Somatomedin
|
|
Igf1 Resistance
|
Resistance To Insulin-Like Growth Factor I
|
|
Resistance To Somatomedin-C
|
Insulin-Like Growth Factor 1, Resistance To
|
|
|
| Leiomyosarcoma |
|
|
| Sotos Syndrome |
|
Cerebral Gigantism
|
SOTOS
|
|
Chromosome 5q35 Deletion Syndrome
|
Sotos Syndrome 1, Formerly
|
|
Sotos1, Formerly
|
Distinctive Facial Appearance, Overgrowth In Childhood, And Learning Disabilities Or Delayed Development
|
|
Sotos Sequence
|
Sotos' Syndrome
|
|
Sotos1
|
Sotos Syndrome 1
|
|
|
| Leiomyoma |
|
Leiomyomatous Neoplasm
|
Leiomyomatous Tumor
|
|
Leiomyomas
|
Fibroid Tumor
|
|
Uterine Fibroids
|
|
|
| Rhabdoid Cancer |
|
Rhabdoid Tumor
|
Malignant Rhabdoid Tumor
|
|
Malignant Rhabdoid Tumour
|
Rhabdoid Sarcoma
|
|
Rhabdoid Tumor Predisposition Syndrome 1
|
Rhabdoid Tumor Predisposition Syndrome 2
|
|
Atypical Teratoid Rhabdoid Tumor
|
Brain Tumor, Posterior Fossa, Of Infancy, Familial
|
|
Atypical Teratoid/Rhabdoid Tumor
|
|
|
| Adrenal Cortical Adenoma |
|
Adrenocortical Adenoma
|
Adenoma Adrenocortical
|
|
|
| Adrenal Cortical Carcinoma |
|
Adrenocortical Carcinoma
|
Adrenal Cortex Carcinoma
|
|
Carcinoma Of The Adrenal Cortex
|
Acc
|
|
Adrenocortical Cancer
|
Carcinoma Adrenocortical
|
|
|
| Hyperandrogenism |
|
Hyperandrogenization Syndrome
|
|
|
| Seminoma |
|
|
| Hyperinsulinism |
|
|
| Adult Syndrome |
|
Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome
|
Acro Dermato Ungual Lacrimal Tooth Syndrome
|
|
Pigment Anomaly-Ectrodactyly-Hypodontia Syndrome
|
Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome
|
|
Adult
|
|
|
| Androgen Insensitivity Syndrome |
|
Androgen Resistance Syndrome
|
AIS
|
|
Testicular Feminization Syndrome
|
Androgen Receptor Deficiency
|
|
Dhtr Deficiency
|
Dihydrotestosterone Receptor Deficiency
|
|
Ar Deficiency
|
Testicular Feminization
|
|
Tfm
|
Androgen Insensitivity
|
|
Androgen-Insensitivity Syndrome
|
Goldberg-Maxwell Syndrome
|
|
Complete Androgen Insensitivity Syndrome
|
Cais
|
|
Feminisation - Testicular
|
Goldberg - Maxwell Syndrome
|
|
Androgen Insensitivity Syndrome, Complete
|
Morris Syndrome
|
|
Ary
|
AR
|
|
Insensitivity Syndrome, Androgen
|
Androgen Insensitivity Nos
|
|
|
| Umbilical Hernia |
|
|
| Blastoma |
|
|
| Insulinoma |
|
Islet Cell Adenoma
|
Insulin-Producing Tumor Of Islet Cells
|
|
Adenoma Islet Cell
|
Islet Cell Tumor
|
|
Experimental Organism Islet Cell Adenoma Neoplasm
|
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Male Breast Cancer
|
|
Breast Cancer, Familial
|
Malignant Neoplasm Of Breast
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Omphalocele |
|
Omphalocoele
|
Congenital Omphalocele
|
|
Exomphalos
|
Exumbilication
|
|
|
| Wilms Tumor 5 |
|
Wilms Tumor
|
WT5
|
|
Wilms Tumor Susceptibility-5
|
Wilms Tumor And Radial Bilateral Aplasia
|
|
Nephroblastoma
|
Wilms' Tumor
|
|
Wilms Tumor, Susceptibility To
|
Wtsl
|
|
Bilateral Radial Aplasia With Wilms Tumor
|
Embryonal Adenosarcoma
|
|
Embryonal Nephroma
|
Kidney Wilms Tumor
|
|
Kidney, Adenomyosarcoma, Embryonal
|
Kidney, Carcinosarcoma, Embryonal
|
|
Kidney, Embryoma
|
Kidney, Embryonal Mixed Tumor
|
|
Nephroma
|
Renal Adenosarcoma
|
|
Renal Cancer, Wilms
|
Renal Wilms Tumor
|
|
Tumor, Wilms
|
Hereditary Susceptibility To Wilms Tumor 5
|
|
|
| Clear Cell Sarcoma |
|
Sarcoma, Clear Cell
|
Adult Soft Part Clear Cell Sarcoma
|
|
Clear Cell Sarcoma Of Soft Parts
|
Malignant Melanoma Of Soft Parts
|
|
Malignant Melanoma Of Soft Tissues
|
Melanoma, Malignant, Of Soft Parts
|
|
Sarcoma Clear Cell
|
|
|
| Ewing Sarcoma |
|
Neuroepithelioma
|
Ewing'S Tumor
|
|
Primitive Neuroectodermal Tumor
|
Ewings Sarcoma
|
|
Ewing'S Sarcoma
|
Peripheral Neuroepithelioma
|
|
ES
|
Ewings Sarcoma-Primitive Neuroectodermal Tumor
|
|
Localized Peripheral Primitive Neuroectodermal Tumor
|
Peripheral Primitive Neuroectodermal Tumor
|
|
Ewing Tumor
|
Sarcoma, Ewing'S
|
|
Ewing Family Of Tumors
|
Extraosseous Ewing Tumor
|
|
Askin Tumor
|
Ewing'S Family Localized Tumor
|
|
Ewing'S Sarcoma/Peripheral Primitive Neuroectodermal Tumor
|
Localized Ewing Sarcoma
|
|
Localized Ewing'S Sarcoma
|
Localized Ewing'S Sarcoma/Peripheral Primitive Neuroectodermal Tumor
|
|
Localized Ewing'S Tumor
|
Pnet Of Thoracopulmonary Region
|
|
Tumor Of The Ewing Family
|
Skeletal Ewing Sarcoma
|
|
Osseous Ewing Sarcoma
|
Ppnet
|
|
Peripheral Pnet
|
Extraskeletal Ewing Sarcoma
|
|
Eoe
|
Extraosseous Ewing Sarcoma
|
|
Extraskeletal Ewing Tumor
|
Esft
|
|
Ewing Sarcoma Family Of Tumors
|
Pne
|
|
Pnet
|
Pnet Of The Chest Wall
|
|
Sarcoma, Ewing
|
Neuroectodermal Tumors, Primitive, Peripheral
|
|
Neuroectodermal Tumor, Primitive
|
Disorder Of Eye
|
|
Askin'S Tumor
|
Extraosseous Ewings Sarcoma-Primitive Neuroepithelial Tumor
|
|
Neuroepithelioma, Peripheral
|
|
|
| Papilloma Of Choroid Plexus |
|
Choroid Plexus Papilloma
|
CPP
|
|
Childhood Choroid Plexus Papilloma
|
Papilloma Choroid Plexus
|
|
Papilloma, Choroid Plexus
|
Choroid Plexus Carcinoma
|
|
|
| Chronic Fatigue Syndrome |
|
Myalgic Encephalomyelitis
|
Postviral Fatigue Syndrome
|
|
Cfs
|
Myalgic Encephalitis
|
|
Encephalomyelitis, Myalgic
|
Chronic Fatigue
|
|
Fatigue Syndrome, Chronic
|
Benign Myalgic Encephalomyelitis
|
|
Akureyri
|
Akureyri Disease
|
|
Cfs - [Chronic Fatigue Syndrome]
|
Epidemic Neuromyasthenia
|
|
Myalgic Encephalomyelitis Syndrome
|
Me - [Myalgic Encephalomyelitis]
|
|
Pvfs - [Postviral Fatigue Syndrome]
|
Neuromyasthenia
|
|
Iceland Disease
|
Icelandic Disease
|
|
|
| Spastic Paraplegia 17, Autosomal Dominant |
|
Silver Syndrome
|
SPG17
|
|
Silver Spastic Paraplegia Syndrome
|
Spastic Paraplegia With Amyotrophy Of Hands And Feet
|
|
Hereditary Spastic Paraplegia 17
|
Autosomal Dominant Spastic Paraplegia Type 17
|
|
Spastic Paraplegia 17
|
Spastic Paraplegia-Amyotrophy Of Hands And Feet
|
|
Autosomal Dominant Spastic Paraplegia 17
|
Dhmn5b
|
|
Distal Hereditary Motor Neuropathy Type 5b
|
Paraplegia, Spastic, Autosomal Dominant, Type 17
|
|
Russell-Silver Syndrome
|
Neuronopathy, Distal Hereditary Motor, Type Vb
|
|
|
| Choriocarcinoma |
|
|
| Turner Syndrome |
|
Monosomy X
|
Gonadal Dysgenesis Turner Type
|
|
Ullrich-Turner Syndrome
|
Bonnevie-Ullrich Syndrome
|
|
Karyotype 45, X
|
Genital Dwarfism, Turner Type
|
|
Gonadal Dysgenesis
|
45,X
|
|
Turner'S Syndrome
|
Gonadal Dysgenesis - Turner
|
|
Monosomy X Syndrome
|
Xo Syndrome
|
|
Genital Dwarfism
|
45, X Syndrome
|
|
Bonnevie-Ulrich Syndrome
|
Chromosome X Monosomy X
|
|
Schereshevkii Turner Syndrome
|
Turner Varny Syndrome
|
|
Ts
|
45,X Syndrome
|
|
45,X/46,Xx Syndrome
|
Turners Syndrome
|
|
Gonadal Dysgenesis, 45,X
|
X0 Syndrome
|
|
|
| Type 1 Diabetes Mellitus |
|
Diabetes Mellitus, Insulin-Dependent
|
Diabetes Mellitus Type 1
|
|
IDDM
|
Type 1 Diabetes
|
|
Insulin-Dependent Diabetes Mellitus
|
T1D
|
|
Juvenile-Onset Diabetes
|
Jod
|
|
Diabetes Mellitus, Type 1
|
Diabetes Mellitus, Insulin-Dependent-1
|
|
Type I Diabetes Mellitus
|
Autoimmune Diabetes
|
|
Juvenile Diabetes
|
Juvenile-Onset Diabetes Mellitus
|
|
Diabetes, Insulin Dependent
|
Insulin-Dependent Diabetes Mellitus-1
|
|
Diabetes Mellitus Insulin-Dependent
|
Diabetes Autoimmune
|
|
Diabetes Mellitus, Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 1, Susceptibility To
|
|
Diabetes Type 1
|
Type I Diabetes
|
|
Diabetes, Autoimmune
|
T1dm - [Type 1 Diabetes Mellitus]
|
|
Iddm - [Insulin Dependent Diabetes Mellitus]
|
Type 1 Iddm
|
|
Juvenile Diabetes Mellitus Without Compications
|
Idiopathic Insulin-Dependent Diabetes Mellitus Without Complications
|
|
Juvenile-Onset Diabetes Mellitus Without Compications
|
Ketosis-Prone Diabetes Mellitus Without Compications
|
|
Juvenile-Onset-Type Diabetes Mellitus Without Compications
|
|
|
| Embryonal Rhabdomyosarcoma |
|
Rhabdomyosarcoma, Embryonal
|
Rhabdomyosarcoma Embryonal
|
|
Botryoid Rhabdomyosarcoma
|
Erms
|
|
Spindle Cell Rhabdomyosarcomas
|
|
|
| Adrenal Adenoma |
|
Adenoma Of The Adrenal Gland
|
Adrenal Incidentaloma
|
|
Adrenal Cortical Adenoma
|
Adrenocortical Adenoma
|
|
|
| Meninges Hemangiopericytoma |
|
Hemangiopericytoma Of Meninges
|
Meningeal Hemangiopericytoma
|
|
|
| Chronic Kidney Disease |
|
Chronic Renal Disease
|
Chronic Kidney Failure
|
|
Ckd
|
Chronic Renal Failure
|
|
Kidney Failure, Chronic
|
Chronic Renal Failure Syndrome
|
|
Crf
|
Renal Failure - Chronic
|
|
Renal Failure Chronic
|
Chronic Kidney Diseases
|
|
Chronic Kidney Disease Stage 5
|
Ckd - [Chronic Kidney Disease]
|
|
Crf - [Chronic Renal Failure]
|
Chronic Kidney Impairment
|
|
Chronic Renal Impairment
|
Chronic Kidney Shutdown
|
|
Chronic Hypoxic Kidney Failure
|
Chronic Kidney Collapse
|
|
Chronic Renal Insufficiency
|
Chronic Kidney Toxaemia
|
|
Chronic Kidney Hypofunction
|
Chronic Renal Suppression
|
|
Chronic Renal Failure, Stage 5
|
Ckd - [Chronic Kidney Disease] Stage 5
|
|
End Stage Kidney Failure
|
End Stage Renal Failure
|
|
End Stage Kidney Disease
|
End Stage Renal Disease
|
|
End Stage Chronic Renal Failure
|
Esrf - [End Stage Renal Failure]
|
|
Esrd - [End Stage Renal Diseases]
|
Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
|
|
|
| Prader-Willi Syndrome |
|
Prader-Labhart-Willi Syndrome
|
PWS
|
|
Willi-Prader Syndrome
|
Prader-Willi Syndrome Due To Translocation
|
|
Prader-Willi Syndrome Due To Imprinting Mutation
|
Prader-Willi Syndrome Due To Maternal Uniparental Disomy Of Chromosome 15
|
|
Prader Willi Syndrome
|
Upd(15)Mat
|
|
|
| Neural Tube Defects |
|
Spina Bifida
|
Neural Tube Defect
|
|
NTD
|
Neural Tube Defects, Susceptibility To
|
|
Spinal Dysraphism
|
Spina Bifida, Susceptibility To
|
|
Rachischisis
|
Cleft Spine
|
|
Open Spine
|
Hydrocele Spinalis
|
|
Neural Tube Defect Nos
|
Sb - [Spina Bifida]
|
|
Spinal Hernia Nos
|
Spinal Fissure Nos
|
|
|
| Smooth Muscle Tumor |
|
|
| Medulloblastoma |
|
MDB
|
Cpnet
|
|
Localized Primitive Neuroectodermal Tumor
|
Classic Medulloblastoma
|
|
Medulloblastoma Predisposition Syndrome
|
Medulloblastoma, Somatic
|
|
Brain Medulloblastoma
|
Cns Pnet
|
|
Infratentorial Primitive Neuroectodermal Tumor
|
Neuroectodermal Tumors, Primitive
|
|
Medulloblastomas
|
Desmoplastic Medulloblastoma
|
|
Medulloblastoma, With Extensive Nodularity
|
Medulloblastoma Of Unspecified Site
|
|
Medullomyoblastoma Of Unspecified Site
|
|
|
| Lymphangioleiomyomatosis |
|
Lymphangiomyomatosis
|
LAM
|
|
Lung Lymphangioleiomyomatosis
|
Pulmonary Lymphangioleiomyomatosis
|
|
Lymphangioleiomyomatosis, Somatic
|
Lymphangio-Myomatosis
|
|
|
| Endometrial Cancer |
|
Endometrial Carcinoma
|
Endometrial Neoplasm
|
|
Malignant Neoplasm Of Endometrium
|
Endometrioid Carcinoma
|
|
Endometrial Neoplasms
|
Carcinoma, Endometrioid
|
|
Endometrial Cancer, Familial
|
Endometrial Carcinoma, Somatic
|
|
Endometrial Cancer, Susceptibility To
|
Endometrial Ca
|
|
Malignant Endometrial Neoplasm
|
Neoplasm Of Endometrium
|
|
Primary Malignant Neoplasm Of Endometrium
|
Tumor Of Endometrium
|
|
Carcinoma Of The Endometrium
|
Endometrioid Carcinoma Of Female Reproductive System
|
|
ENDMC
|
Carcinoma Endometrioid
|
|
Endometrial Cancers
|
Cancer, Endometrial
|
|
Uterine Corpus Cancer
|
|
|
| Intellectual Developmental Disorder, X-Linked, Syndromic, Wilson-Turner Type |
|
Wilson-Turner Syndrome
|
WTS
|
|
Mrxs6
|
X-Linked Intellectual Disability-Gynecomastia-Obesity Syndrome
|
|
Mrxswt
|
Wilson-Turner X-Linked Mental Retardation Syndrome
|
|
Mental Retardation, X-Linked, Syndromic 6
|
Mental Retardation, X-Linked, With Gynecomastia And Obesity
|
|
Intellectual Disability, X-Linked, Syndromic 6
|
Intellectual Disability, X-Linked, With Gynecomastia And Obesity
|
|
Wilson Turner Intellectual Disability Syndrome
|
X-Linked Intellectual Disability - Gynecomastia - Obesity
|
|
|
| Breast Disease |
|
|
| Adrenal Cortex Disease |
|
|
| Islet Cell Tumor |
|
Pancreatic Neuroendocrine Tumor
|
Neuroendocrine Tumor Of Pancreas
|
|
Pnet
|
Pancreatic Net
|
|
Pancreatic Endocrine Tumor
|
Well-Differentiated Nen Of Pancreas
|
|
Well-Differentiated Neuroendocrine Neoplasm Of Pancreas
|
Well-Differentiated Pancreatic Nen
|
|
Well-Differentiated Pancreatic Neuroendocrine Neoplasm
|
Endocrine Pancreas Cancer
|
|
Islet Cell Neoplasm
|
Islet Cell Tumour
|
|
Malignant Pancreatic Endocrine Tumor
|
Malignant Pancreatic Endocrine Tumour
|
|
Malignant Tumor Of Endocrine Pancreas
|
Malignant Tumour Of Endocrine Pancreas
|
|
Pancreatic Endocrine Neoplasm
|
Pancreatic Neuroendocrine Neoplasm
|
|
Adenoma, Islet Cell
|
Well Differentiated Pancreatic Endocrine Tumor
|
|
Malignant Neoplasm Of Endocrine Pancreas
|
Pancreatic Endocrine Carcinoma
|
|
|
| Hemangioma |
|
|
| Asperger Syndrome |
|
Asperger Disorder
|
Asperger Syndrome, Susceptibility To
|
|
|
| Prostate Cancer |
|
Prostate Carcinoma
|
Prostate Cancer, Familial
|
|
Prostate Neoplasm
|
Prostate Cancer, Somatic
|
|
Prostate Cancer, Susceptibility To
|
Prostatic Cancer
|
|
Prostatic Neoplasms
|
Hereditary Prostate Cancer
|
|
Prostatic Neoplasm
|
Cancer Of Prostate
|
|
Carcinoma Of Prostate
|
Familial Prostate Cancer
|
|
Familial Prostate Carcinoma
|
Malignant Tumor Of Prostate
|
|
Malignant Neoplasm Of Prostate
|
Prostate Cancer, Familial, Susceptibility To
|
|
Malignant Tumor Of The Prostate
|
Ngp - New Growth Of Prostate
|
|
Tumor Of The Prostate
|
Prostate Cancer, Hereditary
|
|
Cancer Of The Prostate
|
Malignant Neoplasm Of The Prostate
|
|
Prostatic Carcinoma
|
PC
|
|
Prca
|
Cancer, Prostate
|
|
Malignant Prostatic Tumour
|
Malignant Tumour Of Prostate
|
|
Primary Prostate Cancer
|
Primary Malignant Neoplasm Of Prostate
|
|
Prostate Gland Cancer
|
|
|
| Glycogen Storage Disease |
|
Glycogenosis
|
Glycogenoses
|
|
Gsd
|
Storage Disease, Glycogen
|
|
Gsd - [Glycogen Storage Disease]
|
Glycogen Thesaurismosis
|
|
Diffuse Glycogenosis
|
Generalised Glycogen Storage Disease
|
|
Generalised Glycogenosis
|
Generalised Glycogen Storage Disease Of Infants
|
|
Glycogen Synthase Deficiency
|
|
|
| Endosteal Hyperostosis, Autosomal Dominant |
|
Osteosclerosis
|
Worth Syndrome
|
|
Osteosclerosis, Autosomal Dominant
|
Hyperostosis, Endosteal
|
|
Endosteal Hyperostosis, Worth Type
|
Worth Disease
|
|
Autosomal Dominant Endosteal Hyperostosis
|
Autosomal Dominant Osteosclerosis, Worth Type
|
|
Hyperostosis Corticalis Generalisata, Benign Form Of Worth, With Torus Palatinus
|
Autosomal Dominant Osteosclerosis
|
|
Benign Form Of Worth Hyperostosis Corticalis Generalisata With Torus Platinus
|
Worth'S Syndrome
|
|
Worth Type Autosomal Dominant Osteosclerosis
|
Hyperostosis Corticalis Generalisata, Benign Form Of Worth With Torus Palatinus
|
|
Osteosclerosis, Autosomal Dominant, Worth Type
|
WENHY
|
|
Endosteal Hyperostosis Autosomal Dominant
|
Hyperostosis Corticalis Generalisata Benign Form Of Worth With Torus Palatinus
|
|
Osteosclerosis Autosomal Dominant
|
Acquired Osteosclerosis
|
|
|
| Paraganglioma |
|
Chemodectoma
|
Glomus Body Tumor
|
|
Paragangliomas
|
Carotid Body Paraganglioma
|
|
Extra-Adrenal Paraganglioma
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Hyperinsulinemic Hypoglycemia, Familial, 2 |
|
Persistent Hyperinsulinemic Hypoglycemia Of Infancy
|
Phhi
|
|
Familial Hyperinsulinism
|
Congenital Hyperinsulinism
|
|
HHF2
|
Nesidioblastosis
|
|
Hyperinsulinemic Hypoglycemia Due To Focal Adenomatous Hyperplasia
|
Familial Hyperinsulinemic Hypoglycemia 2
|
|
Autosomal Recessive Hyperinsulinemic Hypoglycemia Due To Kir6.2 Deficiency
|
Chi
|
|
Congenital Isolated Hyperinsulinism
|
Hyperinsulinemic Hypoglycemia, Persistent
|
|
Hyperinsulinism, Neonatal
|
Hyperinsulinism, Congenital
|
|
Hyperinsulinism, Familial
|
Hyperinsulinemic Hypoglycemia Familial
|
|
Hyperinsulinism Congenital
|
Hyperinsulinism Familial With Pancreatic Nesidioblastosis
|
|
Hypoglycemia Hyperinsulinemic Of Infancy
|
Nesidioblastosis Of Pancreas
|
|
Hyperinsulinemic Hypoglycemia Familial 2
|
Hyperinsulinemia Hypoglycemia Of Infancy
|
|
Infancy Hyperinsulinemia Hypoglycemia
|
Neonatal Hyperinsulinism
|
|
Persistent Hyperinsulinemia Hypoglycemia Of Infancy
|
Persistent Hyperinsulinemic Hypoglycemia
|
|
Phhi Hypoglycemia
|
Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency
|
|
Autosomal Dominant Hyperinsulinemic Hypoglycemia Due To Kir6.2 Deficiency
|
Dominant Katp Hyperinsulinism Due To Kir6.2 Deficiency
|
|
Diazoxide-Resistant Focal Hyperinsulinism Due To Kir6.2 Deficiency
|
Hyperinsulinemic Hypoglycemia Due To Kir6.2 Deficiency, Diazoxide-Resistant Focal Form
|
|
Fhi
|
Familial Hyperinsulinemic Hypoglycemia
|
|
Autosomal Recessive Hyperinsulinism Due To Kir6.2 Deficiency
|
Hypoglycemia, Hyperinsulinemic, Familial, Type 2
|
|
Hi-C
|
|
|
| Type 2 Diabetes Mellitus |
|
Insulin Resistance
|
NIDDM
|
|
Type 2 Diabetes
|
Diabetes Mellitus, Non-Insulin-Dependent
|
|
T2D
|
Noninsulin-Dependent Diabetes Mellitus
|
|
Diabetes Mellitus, Type Ii
|
Maturity-Onset Diabetes
|
|
Insulin Resistance, Severe, Digenic
|
Diabetes Mellitus, Type 2
|
|
Diabetes Mellitus, Noninsulin-Dependent
|
Diabetes Mellitus, Noninsulin-Dependent, Association With
|
|
Diabetes Mellitus, Noninsulin-Dependent, Late Onset
|
Hypertension, Insulin Resistance-Related, Susceptibility To
|
|
Insulin Resistance, Susceptibility To
|
Non-Insulin-Dependent Diabetes Mellitus
|
|
Type Ii Diabetes Mellitus
|
Adult-Onset Diabetes Mellitus
|
|
Maturity-Onset Diabetes Mellitus
|
Diabetes Mellitus Type 2
|
|
Type Ii Diabetes
|
Type 2 Diabetes Mellitus, Susceptibility To
|
|
Diabetes, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
|
|
Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 2, Susceptibility To
|
|
Diabetes Mellitus, Noninsulin-Dependent, 2
|
Diabetes Mellitus, Type Ii, Susceptibility To
|
|
Hypertension, Insulin Resistance-Related
|
Adult-Onset Diabetes
|
|
Aodm
|
Diabetes Mellitus, Adult-Onset
|
|
Diabetes Mellitus Type Ii
|
Diabetes Mellitus Type 2, Susceptibility To
|
|
Diabetes, Type Ii, Susceptibility To
|
Diabetes Type 2
|
|
Diabetes Mellitus
|
Adult Onset Diabetes
|
|
Maturity Onset Diabetes
|
Nonketotic Diabetes
|
|
Non-Insulin Dependent Diabetes Mellitus
|
T2dm - [Type 2 Diabetes Mellitus]
|
|
Niddm - [Non Insulin Dependent Diabetes Mellitus]
|
Dm2
|
|
Dm Type Ii
|
Diabetic Type 2
|
|
Insulin Requiring Type 2 Diabetes
|
Noninsulin Dependent Diabetes
|
|
Non-Insulin-Dependent Diabetes Mellitus Without Complications
|
Diabetes Due To Insulin Secretory Defect
|
|
Diabetes Mellitus Due To Insulin Secretory Defect
|
Non-Insulin-Dependent Diabetes Of The Young
|
|
Senile Diabetes
|
Nonketotic Hyperglycaemia
|
|
Stable Diabetes
|
|
|
| Sarcoma, Synovial |
|
Synovial Sarcoma
|
Synovialosarcoma
|
|
Synovial Cell Sarcoma
|
Sarcoma Synovial
|
|
|
| Hepatocellular Carcinoma |
|
Liver Cancer
|
Primary Liver Cancer
|
|
HCC
|
Hepatoma
|
|
Malignant Neoplasm Of Liver
|
Liver Neoplasms
|
|
Cancer, Hepatocellular
|
Liver Cell Carcinoma
|
|
Lcc
|
Hepatoblastoma, Somatic
|
|
Hepatic Cancer
|
Primary Malignant Neoplasm Of Liver
|
|
Rare Tumor Of Liver And Intrahepatic Biliary Tract
|
Hepatocellular Carcinoma, Somatic
|
|
Hepatocellular Carcinoma, Childhood Type, Somatic
|
Hepatocellular Cancer, Somatic
|
|
Ca Liver - Primary
|
Hepatic Neoplasm
|
|
Malignant Hepato-Biliary Neoplasm
|
Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary
|
|
Malignant Neoplasm Of Liver, Primary
|
Malignant Tumor Of Liver
|
|
Neoplasm Of Liver
|
Non-Resectable Primary Hepatic Malignant Neoplasm
|
|
Resectable Malignant Neoplasm Of Liver
|
Resectable Malignant Neoplasm Of The Liver
|
|
Primary Liver Carcinoma
|
Primary Malignant Liver Neoplasm
|
|
Primary Cancer Of Liver
|
Primary Tumor Of The Liver
|
|
Rare Tumor Of Liver And Ibt
|
Hepatocellular Cancer
|
|
Neoplasm Of The Liver
|
Carcinoma, Hepatocellular
|
|
Hepatomas
|
Liver Neoplasm
|
|
Liver Carcinoma
|
Liver And Intrahepatic Biliary Tract Carcinoma
|
|
Malignant Hepatobiliary Neoplasm
|
Adult Primary Hepatocellular Carcinoma
|
|
Hepatoblastoma
|
Carcinoma Of Liver
|
|
Malignant Liver Tumour
|
Malignant Hepatic Tumour
|
|
|
| Type 1 Diabetes Mellitus 8 |
|
Diabetes Mellitus, Insulin-Dependent, 8
|
Iddm8
|
|
Insulin-Dependent Diabetes Mellitus 8
|
T1D8
|
|
Insulin-Dependent Diabetes Mellitus-8
|
|
|
| Meningioma, Familial |
|
Meningioma
|
Familial Meningioma
|
|
Meningioma, Familial, Susceptibility To
|
Meningeal Neoplasm
|
|
Meningeal Neoplasms
|
Meningiomas
|
|
Meningioma, Nf2-Related, Somatic
|
Meningioma, Sis-Related
|
|
Meningothelial Cell Tumor
|
Neoplasm Of The Meninges
|
|
Primary Meningeal Tumor
|
Familial Multiple Meningioma
|
|
MNGMA
|
Meningioma, Benign, No Icd-O Subtype
|
|
Intracranial Meningioma
|
Meningothelial Cell Neoplasm
|
|
Supratentorial Meningioma
|
Primary Neoplasm Of Spinal Meninges
|
|
Benign Intracranial Meningioma
|
Benign Meningioma
|
|
Meningeal Tumours
|
Meningeal Sarcoma Of Unspecified Site
|
|
Meningothelial Sarcoma Of Unspecified Site
|
|
|
| Temple Syndrome |
|
Uniparental Disomy, Maternal, Chromosome 14
|
Temple Syndrome Due To Paternal 14q32.2 Microdeletion
|
|
Paternal Del(14)(Q32.2)
|
Temple Syndrome Due To Paternal 14q32.2 Hypomethylation
|
|
Temple Syndrome Due To Maternal Uniparental Disomy Of Chromosome 14
|
Upd(14)Mat
|
|
|
| Skeletal Muscle Cancer |
|
Malignant Tumor Of Skeletal Muscle
|
Skeletal Muscle Neoplasm
|
|
|
| Transient Neonatal Diabetes Mellitus |
|
Diabetes Mellitus, Transient Neonatal
|
Tndm
|
|
Chromosome 6-Associated Transient Diabetes Mellitus
|
Dmtn
|
|
Diabetes Mellitus, 6q24-Related Transient Neonatal
|
Tndm1
|
|
Neonatal Diabetes Mellitus, Transient
|
Tndm -[Transient Neonatal Diabetes Mellitus]
|
|
|
| Benign Fibrous Mesothelioma |
|
Fibrous Mesothelioma, Benign
|
Localized Benign Fibrous Mesothelioma
|
|
Solitary Fibrous Tumor, Pleural
|
Pleural Solitary Fibrous Tumor
|
|
Solitary Fibrous Tumor
|
|
|
| Rett Syndrome |
|
Atypical Rett Syndrome
|
RTT
|
|
Rett Disorder
|
Rts
|
|
Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use
|
Rett Syndrome, Preserved Speech Variant
|
|
Rett Syndrome, Atypical
|
Rett'S Disorder
|
|
Rett Syndrome Variant
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome
|
|
Cerebroatrophic Hyperammonemia
|
Rett Like Syndrome
|
|
Rett'S Syndrome
|
Atypical Rtt
|
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use
|
Rett Syndrome Preserved Speech Variant
|
|
Rett Syndrome Zappella Variant
|
Rett Syndrome, Zappella Variant
|
|
|
| Glioblastoma |
|
Glioblastoma Multiforme
|
Gbm
|
|
Adult Glioblastoma Multiforme
|
Grade Iv Adult Astrocytic Tumor
|
|
Primary Glioblastoma Multiforme
|
Spongioblastoma Multiforme
|
|
Adult Glioblastoma
|
Primary Glioblastoma
|
|
|
| Pheochromocytoma |
|
Pheochromocytoma, Susceptibility To
|
Phaeochromocytoma
|
|
Adrenal Gland Chromaffin Paraganglioma
|
Adrenal Gland Chromaffinoma
|
|
Adrenal Gland Paraganglioma
|
Adrenal Gland Pheochromocytoma
|
|
Chromaffin Paraganglioma Of The Adrenal Gland
|
Intraadrenal Paraganglioma
|
|
PCC
|
Chromaffin Cell Tumor
|
|
Medullary Chromaffinoma
|
Medullary Paraganglioma
|
|
Pheochromoblastoma
|
Pheochromocytomas
|
|
Chromaffin Cell Neoplasm
|
Pheochromocytoma, Malignant
|
|
|
| Hyperpituitarism |
|
|
| Paralytic Lagophthalmos |
|
|
| Ovarian Cancer |
|
Ovarian Carcinoma
|
Ovarian Neoplasm
|
|
Malignant Tumour Of Ovary
|
Cancer Of The Ovary
|
|
Epithelial Ovarian Cancer
|
Neoplasm Of Ovary
|
|
Ovarian Neoplasms
|
Ovarian Cancers
|
|
Malignant Neoplasm Of Ovary
|
Primary Malignant Neoplasm Of Ovary
|
|
Ovarian Cancer, Somatic
|
Malignant Ovarian Tumor
|
|
Ovary Neoplasm
|
Primary Ovarian Cancer
|
|
Tumor Of The Ovary
|
Malignant Neoplasm Of The Ovary
|
|
Malignant Tumor Of The Ovary
|
Ovarian Malignant Tumor
|
|
OC
|
Ovarian Carcinomas
|
|
Cancer, Ovarian
|
Cancer Of Ovary
|
|
Ovary Cancer
|
Ca Ovary
|
|
|
| Muscle Cancer |
|
Myosarcoma
|
Malignant Neoplasm Of Muscle
|
|
Malignant Tumor Of Muscle
|
Malignant Tumor Of The Muscle
|
|
Muscle Neoplasms
|
Myomatous Neoplasm
|
|
|
| Osteogenic Sarcoma |
|
Osteosarcoma
|
OSRC
|
|
Osteosarcoma, Somatic
|
Neoplasms, Bone Tissue
|
|
Bone Tissue Neoplasm
|
Osteoid Sarcoma
|
|
Skeletal Sarcoma
|
Osteosarcoma Of Bone
|
|
Bone Sarcoma
|
|
|
| Choline Deficiency Disease |
|
|
| Pre-Eclampsia |
|
Preeclampsia
|
Gestational Hypertension
|
|
Hypertension Induced By Pregnancy
|
Pre-Eclamptic Toxaemia
|
|
Pregnancy Associated Hypertension
|
Proteinuric Hypertension Of Pregnancy
|
|
Hypertension, Pregnancy-Induced, Susceptibility To
|
Preeclampsia/Eclampsia
|
|
Pregnancy Toxemia
|
Toxaemia Of Pregnancy
|
|
Gestational Proteinuric Hypertension
|
Pregnancy-Induced Hypertension
|
|
Toxemia Of Pregnancy
|
Preeclampsia, Susceptibility To
|
|
Transient Hypertension Of Pregnancy
|
Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria
|
|
Gestational Hypertension Nos
|
Mild Proteinuric Hypertension Of Pregnancy
|
|
Pih - [Pregnancy-Induced Hypertension]
|
Pregnancy-Induced Hypertension Nos
|
|
Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria
|
Pe - [Pre-Eclampsia]
|
|
Pre-Eclampsia Nos
|
Pre-Eclamptic Nos
|
|
Pregnancy Pre-Eclampsia
|
Puerperal Pre-Eclampsia
|
|
Pre-Eclampsia Toxaemia
|
Toxaemia In Pregnancy
|
|
Pet - [Pre-Eclamptic Toxaemia]
|
Maternal Toxaemia
|
|
|
| Persistent Fetal Circulation Syndrome |
|
Persistent Fetal Circulation
|
Fetal Circulation
|
|
Persistent Pulmonary Hypertension Of The Newborn
|
Congenital Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
|
|
Persistent Foetal Circulation
|
Persistent Foetal Circulation Syndrome
|
|
Pfc - [Persistent Fetal Circulation] Syndrome
|
Pphn - [Persistent Pulmonary Hypertension Of The Newborn]
|
|
Newborn Pulmonary Hypertension
|
Primary Pulmonary Hypertension Of Newborn
|
|
|
| Three M Syndrome 1 |
|
3-M Syndrome
|
Yakut Short Stature Syndrome
|
|
3m Syndrome
|
Le Merrer Syndrome
|
|
Dolichospondylic Dysplasia
|
Gloomy Face Syndrome
|
|
Three M Syndrome
|
3M1
|
|
3m Syndrome 1
|
Miller-Mckusick-Malvaux Syndrome
|
|
3-Msbn
|
Three-M Slender-Boned Nanism
|
|
Miller-Mckusick-Malvaux-Syndrome
|
3-M Syndrome 1
|
|
3m Syndrome-1
|
3m Syndrome, Type 1
|
|
Dwarfism
|
Dwarfism Tall Vertebrae
|
|
|
| Renal Hypodysplasia/Aplasia 1 |
|
Renal Agenesis
|
Renal Adysplasia
|
|
Renal Aplasia
|
RHDA1
|
|
Hereditary Renal Aplasia
|
Hra
|
|
Hereditary Urogenital Adysplasia
|
Hypodysplasia/Aplasia, Renal, Type 1
|
|
Congenital Absence Of Kidneys Syndrome
|
Congenital Absence Of Kidney
|
|
Aplastic Kidney
|
|
|
| Lung Cancer |
|
Lung Carcinoma
|
Non-Small Cell Lung Carcinoma
|
|
Lung Cancer, Susceptibility To
|
Lung Cancer, Protection Against
|
|
Adenocarcinoma Of Lung, Somatic
|
Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In
|
|
Nonsmall Cell Lung Cancer
|
Lung Neoplasm
|
|
Carcinoma Of Lung
|
Lung Non-Small Cell Carcinoma
|
|
Non-Small Cell Lung Cancer
|
Nsclc
|
|
Lung Neoplasms
|
Malignant Neoplasm Of Lung
|
|
Alveolar Cell Carcinoma
|
Nonsmall Cell Lung Cancer, Somatic
|
|
Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In
|
Nonsmall Cell Lung Cancer, Susceptibility To
|
|
Lung Cancer, Somatic
|
Lung Cancer, Resistance To
|
|
Cancer Of Lung
|
Cancer Of Bronchus
|
|
Cancer Of The Lung
|
Lung Malignancies
|
|
Lung Malignant Tumors
|
Malignant Lung Tumor
|
|
Malignant Tumor Of Lung
|
Pulmonary Cancer
|
|
Pulmonary Carcinoma
|
Pulmonary Neoplasms
|
|
Respiratory Carcinoma
|
LNCR
|
|
Adenocarcinoma Of Lung
|
Neoplasm Of Lung
|
|
Cancer Lung
|
Carcinoma Non-Small Cell Lung
|
|
Carcinoma, Non-Small-Cell Lung
|
Lung Cancers
|
|
Lung Carcinomas
|
Cancer, Lung
|
|
Cancer, Lung, Non-Small Cell
|
Primary Malignant Neoplasm Of Lung
|
|
Bronchioloalveolar Adenocarcinoma
|
|
|
| Hyperinsulinemic Hypoglycemia |
|
Nesidioblastosis
|
Islet Cell Hyperplasia
|
|
Persistent Hyperinsulinemia Hypoglycemia Of Infancy
|
Hyperinsulinemic Hypoglycaemia
|
|
|
| Small Intestine Leiomyosarcoma |
|
Leiomyosarcoma Of The Small Bowel
|
Smooth Muscle Connective Tissue Tumor
|
|
Leiomyosarcoma Of Small Intestine
|
|
|
| Fetal Alcohol Syndrome |
|
Fetal Alcohol Spectrum Disorders
|
Arbd
|
|
Arnd
|
Alcohol-Related Birth Defects
|
|
Alcohol-Related Neurodevelopmental Disorder
|
Fas
|
|
Fasd
|
Fetus Or Newborn Affected By Alcohol Transmitted Via Placenta Or Breast Milk
|
|
Alcohol Related Birth Defect
|
Alcohol Related Neurodevelopmental Disorder
|
|
Alcohol Affecting Fetus Or Newborn Via Placenta Or Breast Milk
|
Fetus Or Newborn Affected By Alcohol Transmitted Via Placenta And/Or Breast Milk
|
|
Dysmorphism Due To Alcohol
|
Fetal Etoh Syndrome
|
|
|
| Fetal Alcohol Spectrum Disorder |
|
Fetal Alcohol Spectrum Disorders
|
Fetal Alcohol Syndrome
|
|
|
| Pancreatic Cystadenoma |
|
|
| Adrenal Gland Disease |
|
Adrenal Gland Diseases
|
Adrenal Gland Disorders
|
|
|
| Osteoporosis |
|
Postmenopausal Osteoporosis
|
Osteoporosis, Postmenopausal
|
|
Bone Mineral Density Quantitative Trait Locus
|
Bmnd
|
|
Osteoporosis, Involutional
|
Osteoporosis, Susceptibility To
|
|
Osteoporosis, Postmenopausal, Susceptibility
|
Bone Mineral Density Variation Qtl, Osteoporosis
|
|
OSTEOP
|
Involutional Osteoporosis
|
|
Senile Osteoporosis
|
Osteoporosis Postmenopausal
|
|
Bone Mineral Density, Quantitative Trait Locus
|
Osteoporosis, Senile
|
|
Idiopathic Osteoporosis
|
Bone Rarefaction Nos
|
|
Type 1 Osteoporosis
|
|
|
| Syndromic X-Linked Intellectual Disability |
|
X-Linked Syndromic Intellectual Disability
|
|
|
| Neuroblastoma |
|
Nb
|
Neuroblastoma, Susceptibility To
|
|
Neuroblastomas
|
Central Neuroblastoma
|
|
|
| Gastrointestinal System Benign Neoplasm |
|
|
| Gestational Trophoblastic Neoplasm |
|
Hydatidiform Mole
|
Molar Pregnancy
|
|
Gestational Trophoblastic Neoplasia
|
Gestational Trophoblastic Tumor
|
|
Gtn
|
Gestational Trophoblastic Disease
|
|
Gestational Trophoblastic Neoplasms
|
Hydatidiform Mole, Recurrent, 1
|
|
Hydatidiform Mole Benign
|
Trophoblastic Disease
|
|
Trophoblastic Disease Nos
|
Trophoblastic Disorder
|
|
Vesicular Mole Nos
|
Vesicular Mole
|
|
Hydatidiform Mole Nos
|
|
|
| Ovary Leiomyosarcoma |
|
|
| Diabetes Mellitus |
|
|
| Pancreatic Cancer |
|
Pancreatic Carcinoma
|
Carcinoma Of Pancreas
|
|
Familial Pancreatic Carcinoma
|
Pancreatic Neoplasm
|
|
Pancreatic Carcinoma, Familial
|
Malignant Neoplasm Of Pancreas
|
|
Pancreatic Acinar Carcinoma
|
Pancreatic Tumor
|
|
Familial Pancreatic Cancer
|
Neoplasm Of The Pancreas
|
|
Cancer Of The Pancreas
|
Pancreatic Carcinoma, Somatic
|
|
Pancreatic Cancer, Somatic
|
Ca Body Of Pancreas
|
|
Ca Head Of Pancreas
|
Ca Tail Of Pancreas
|
|
Malignant Neoplasm Of Body Of Pancreas
|
Malignant Neoplasm Of Head Of Pancreas
|
|
Malignant Neoplasm Of Tail Of Pancreas
|
Pancreas Neoplasm
|
|
Exocrine Cancer
|
Exocrine Pancreas Carcinoma
|
|
Hereditary Pancreatic Cancer
|
Hereditary Pancreatic Carcinoma
|
|
PNCA
|
Pancreatic Cancer, Susceptibility To
|
|
Carcinoma Of Head Of Pancreas
|
Pancreatic Neoplasms
|
|
Pancreatic Tumors
|
Cancer, Pancreatic
|
|
Cancer Of Pancreas
|
Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site
|
|
|
| Placenta Disease |
|
Placenta Diseases
|
Placenta Disorder
|
|
Pregnancy Complications
|
Placenta Disorders
|
|
|
| Vaginal Adenoma |
|
|
| Li-Fraumeni Syndrome |
|
Sarcoma Family Syndrome Of Li And Fraumeni
|
Sbla Syndrome
|
|
LFS
|
Li-Fraumeni Familiar Cancer Susceptibility Syndrome
|
|
Sarcoma, Breast, Leukaemia And Adrenal Gland Syndrome
|
Lfs1
|
|
Li Fraumeni Syndrome
|
Sarcoma, Breast, Leukemia, And Adrenal Gland Syndrome
|
|
Lfl
|
Sbla Syndrome Li-Fraumeni-Like Syndrome
|
|
Li-Fraumeni Syndrome 1
|
|
|
| Pleural Lipoma |
|
|
| Gastric Cancer |
|
Stomach Cancer
|
Gastric Carcinoma
|
|
Stomach Carcinoma
|
Gastric Cancer, Somatic
|
|
Gastric Neoplasm
|
Carcinoma Of Stomach
|
|
Stomach Neoplasms
|
Malignant Neoplasm Of Stomach
|
|
Gastric Cancer Risk After H. Pylori Infection
|
Cancer Of The Stomach
|
|
Adult Stomach Cancer
|
Adult Stomach Carcinoma
|
|
GASC
|
Gastric Cancer Intestinal
|
|
Gastric Cancers
|
Gastric Carcinomas
|
|
Cancer, Gastric
|
Stomach Neoplasm
|
|
Malignant Neoplasm Of Body Of Stomach
|
Malignant Tumor Of Lesser Curve Of Stomach
|
|
Gastrocarcinoma Of Unspecified Site
|
Leather Bottle Stomach
|
|
Carcinoma Of Fundus Of Stomach
|
Cancer Of Fundus Of Stomach
|
|
Primary Malignant Neoplasm Of Body Of Stomach
|
Cancer Of Body Of Stomach
|
|
Primary Malignant Neoplasm Of Pyloric Antrum
|
Pyloric Antrum Cancer
|
|
Malignant Tumour Of Stomach
|
|
|
| Syndromic Intellectual Disability |
|
|
| Vaginal Benign Neoplasm |
|
|
| Rhabdomyosarcoma 2 |
|
Alveolar Rhabdomyosarcoma
|
Rhabdomyosarcoma, Alveolar
|
|
Rhabdomyosarcoma Alveolar
|
RMS2
|
|
Rmsa
|
Rhabdomyosarcoma 2, Alveolar
|
|
Alveolar Childhood Rhabdomyosarcoma
|
Arms
|
|
Rhabdomyosarcoma, Type 2
|
|
|
| Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome |
|
Wagr Syndrome
|
11p Partial Monosomy Syndrome
|
|
Chromosome 11p13 Deletion Syndrome
|
Wilms Tumor, Aniridia, Genitourinary Anomalies And Mental Retardation Syndrome
|
|
11p Deletion Syndrome
|
Chromosome 11p Deletion Syndrome
|
|
Wagr Complex
|
Wilms Tumor-Aniridia-Genitourinary Anomalies-Intellectual Disability Syndrome
|
|
Deletion 11p13
|
WAGR
|
|
Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Syndrome
|
Chromosome 11p Deletion
|
|
11p Deletion
|
11p Monosomy
|
|
Deletion 11p
|
Monosomy 11p
|
|
Partial Monosomy 11p
|
Agr Triad
|
|
Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome
|
|
Wagr Contiguous Gene Syndrome
|
Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome
|
|
Wilms Tumor-Aniridia-Genitourinary Anomalies-Mr Syndrome
|
Del(11)(P13)
|
|
Monosomy 11p13
|
Chromosome 11, Deletion 11p
|
|
|
| Lynch Syndrome |
|
Hereditary Nonpolyposis Colon Cancer
|
Hereditary Nonpolyposis Colorectal Cancer
|
|
Hereditary Nonpolyposis Colorectal Carcinoma
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
|
Familial Nonpolyposis Colon Cancer
|
Hnpcc
|
|
Coca 1
|
Hereditary Defective Mismatch Repair Syndrome
|
|
Hereditary Non-Polyposis Colon Cancer
|
Hereditary Non-Polyposis Colon Cancer Syndrome
|
|
Hereditary Non-Polyposis Colorectal Cancer
|
Hereditary Non-Polyposis Colorectal Cancer Syndrome
|
|
Hereditary Nonpolyposis Colon Cancer Syndrome
|
Hereditary Nonpolyposis Colorectal Cancer Syndrome
|
|
Hereditary Nonpolyposis Colorectal Neoplasm
|
Hnpcc - Hereditary Nonpolyposis Colon Cancer
|
|
Cancer Family Syndrome
|
Familial Nonpolyposis Colorectal Cancer
|
|
Colon Cancer, Familial Nonpolyposis
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
|
Cancer, Colorectal, Nonpolyposis, Hereditary
|
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
|
|
|
| Gastrointestinal Stromal Tumor |
|
GIST
|
Gastrointestinal Stromal Tumors
|
|
Gastrointestinal Stromal Sarcoma
|
Gastrointestinal Stromal Tumor, Familial
|
|
Gant
|
Gastrointestinal Stromal Tumour
|
|
Stromal Tumor Of Gastrointestinal Tract
|
Stromal Tumour Of Gastrointestinal Tract
|
|
Gastrointestinal Stromal Neoplasm
|
Paraganglioma And Gastric Stromal Sarcoma
|
|
Plexosarcoma
|
|
|
| Hereditary Spastic Paraplegia |
|
Familial Spastic Paraplegia
|
Hereditary Spastic Paraparesis
|
|
Strumpell-Lorrain Disease
|
Familial Spastic Paraparesis
|
|
Hsp
|
Spg
|
|
Strümpell-Lorrain Disease
|
Spastic Paraplegia, Hereditary
|
|
French Settlement Disease
|
Strumpell-Lorrain Syndrome
|
|
Fsp
|
Spastic Paraplegia, Familial
|
|
Spastic Paraplegia Hereditary
|
Spastic Paraplegia 3, Autosomal Dominant
|
|
Spastic Paraparesis
|
Hereditary Spastic Paralysis
|
|
Familial Spastic Paralysis
|
Hereditary Spastic Ataxia
|
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
| Body Mass Index Quantitative Trait Locus 11 |
|
OBESITY
|
Obesity, Susceptibility To
|
|
Leanness, Inherited
|
Obesity, Susceptibility To, Bmiq11
|
|
Obesity, Mild, Early-Onset
|
Obesity, Association With
|
|
Obesity, Early-Onset, Susceptibility To
|
Obesity, Severe
|
|
Obesity, Severe, And Type Ii Diabetes
|
Obesity, Late-Onset
|
|
Obesity , Susceptibility To
|
BMIQ11
|
|
Obesity Bmiq11
|
Obesity, Early-Onset
|
|
Simple Obesity Nos
|
Excess Fat
|
|
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
