| Diseases |
Alias |
|
| Tietz Albinism-Deafness Syndrome |
|
Tietz Syndrome
|
Albinism-Deafness Of Tietz
|
|
Hypopigmentation/Deafness Of Tietz
|
Tietze'S Syndrome
|
|
TADS
|
Costochondral Junction Syndrome
|
|
Costochondritis
|
Tietze Syndrome
|
|
Hypopigmentation-Deafness Syndrome
|
Costalchondritis
|
|
Slipping Rib Syndrome
|
Tietze'S Disease
|
|
Chondropathia Tuberosa
|
Albinism And Complete Nerve Deafness
|
|
Tietz'S Syndrome
|
Hypopigmentation-Hearing Loss Syndrome
|
|
Costal Chondritis
|
Abnormality Of The Costochondral Junction
|
|
|
| Melanoma, Cutaneous Malignant 8 |
|
Melanoma, Cutaneous Malignant, Susceptibility To, 8
|
CMM8
|
|
Melanoma And Renal Cell Carcinoma
|
Melanoma And Renal Cell Carcinoma, Susceptibility To
|
|
Mitf-Related Melanoma And Renal Cell Carcinoma Predisposition Syndrome
|
Cutaneous Malignant Melanoma 8
|
|
Susceptibility To Melanoma And Renal Cell Carcinoma
|
Melanoma, Cutaneous, Malignant, Susceptibility To, Type 8
|
|
|
| Waardenburg Syndrome, Type 2a |
|
Waardenburg Syndrome Type 2a
|
WS2A
|
|
Waardenburg Syndrome, Type Iia
|
Waardenburg Syndrome Without Dystopia Canthorum
|
|
Ws2
|
Waardenburg Syndrome Type Iia
|
|
Waardenburg Syndrome 2a
|
|
|
| Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, And Deafness |
|
Commad Syndrome
|
COMMAD
|
|
Coloboma-Osteopetrosis-Microphthalmia-Macrocephaly-Albinism-Deafness Syndrome
|
|
|
| Heterochromia Iridis |
|
|
| Waardenburg'S Syndrome |
|
Waardenburg Syndrome
|
Van Der Hoeve Halbertsma Waardenburg Gualdi Syndrome
|
|
Van Der Hoeve Halbertsona Waardenburg Syndrome
|
Waardenburg Shah Syndrome
|
|
Waardenburg, Types I And/Or Ii
|
Mende Syndrome
|
|
Waardenburgs Syndrome
|
Waardenburg Syndrome, Type 4a
|
|
|
| Waardenburg Syndrome, Type 2e |
|
Waardenburg Syndrome Type 2
|
Waardenburg Syndrome Type 2e
|
|
WS2E
|
Waardenburg Syndrome, Type 2e, With Or Without Neurologic Involvement
|
|
Waardenburg Syndrome, Type Iie
|
Hypogonadotropic Hypogonadism With Anosmia And Deafness With Or Without Hypopigmentation
|
|
Waardenburg Syndrome Type 2e With Or Without Neurologic Involvement
|
Waardenburg Syndrome Type Iie
|
|
Hypogonadotropic Hypogonadism With Anosmia And Deafness, With Or Without Hypopigmentation
|
Ws2e, With Or Without Neurologic Involvement
|
|
Ws2e With Or Without Neurological Involvement
|
Ws 2
|
|
Ws Type 2
|
Ws2
|
|
Waardenburg Syndrome Type Ii
|
Waardenburg Syndrome 2e
|
|
Kallmann Syndrome And Deafness With Or Without Hypopigmentation
|
Ws2e With Or Without Neurologic Involvement
|
|
Waardenburg Syndrome Type 2e, Without Neurologic Involvement
|
Ws-2
|
|
|
| Waardenburg Syndrome, Type 4a |
|
Waardenburg-Shah Syndrome
|
Shah-Waardenburg Syndrome
|
|
Waardenburg Syndrome Type 4a
|
WS4A
|
|
Ws4
|
Waardenburg Syndrome Type 4
|
|
Waardenburg Syndrome Type Iva
|
Waardenburg Syndrome With Hirschsprung Disease Type 4a
|
|
Hirschsprung Disease With Pigmentary Anomaly
|
Waardenburg-Hirschsprung Syndrome
|
|
Waardenburg Syndrome, Type Iva
|
Waardenburg Syndrome With Hirschsprung Disease, Type 4a
|
|
Waardenburg-Hirschsprung Disease
|
Waardenburg Syndrome, Type 4
|
|
Waardenburg Syndrome 4a
|
|
|
| Ear Malformation |
|
|
| Non-Syndromic Genetic Deafness |
|
Nonsyndromic Genetic Hearing Loss
|
Isolated Genetic Deafness
|
|
Isolated Genetic Hearing Loss
|
Non-Syndromic Genetic Hearing Loss
|
|
|
| Nonsyndromic Hearing Loss |
|
Nonsyndromic Deafness
|
Nonsyndromic Hearing Impairment
|
|
Nonsyndromic Hearing Loss And Deafness
|
Deafness, Nonsyndromic
|
|
Isolated Deafness
|
|
|
| Rare Genetic Deafness |
|
Rare Genetic Hearing Loss
|
|
|
| Inherited Cancer-Predisposing Syndrome |
|
Hereditary Cancer-Predisposing Syndrome
|
|
|
| Bap1 Tumor Predisposition Syndrome |
|
Bap1-Related Tumor Predisposition Syndrome
|
Common Syndrome
|
|
Bap1 Cancer Syndrome
|
Bap1-Tpds
|
|
Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, And Other Internal Neoplasms
|
Tumor Predisposition Syndrome
|
|
Tumor Susceptibility Linked To Germline Bap1 Mutations
|
Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, Other Internal Neoplasms
|
|
Tumor Predisposition
|
|
|
| Microphthalmia |
|
Microphthalmos
|
Isolated Anophthalmia-Microphthalmia Syndrome
|
|
Isolated Microphthalmia-Anophthalmia-Coloboma
|
Simple Microphthalmos
|
|
Clinical Anophthalmia
|
Isolated Anophthalmia - Microphthalmia
|
|
Isolated Pure Microphthalmia
|
Mac Spectrum
|
|
Microphthalmia-Anophthalmia-Coloboma Spectrum
|
Primitive Anophthalmia
|
|
Globe Of Eye Small
|
Small Eyeball
|
|
Hypoplasia Of Eye
|
Isolated Nanophthalmos
|
|
Rudimentary Eye
|
Dysplasia Of Eye
|
|
|
| Clear Cell Papillary Renal Cell Carcinoma |
|
|
| Waardenburg Syndrome, Type 1 |
|
Waardenburg Syndrome Type 1
|
WS1
|
|
Waardenburg Syndrome Type I
|
Waardenburg Syndrome With Dystopia Canthorum
|
|
Waardenburg'S Syndrome Type 1
|
Waardenburg Syndrome 1
|
|
Waardenburg Syndrome, Type I
|
Waardenburg Syndrome
|
|
|
| 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
|
|
|
| Osteopetrosis |
|
Marble Bone Disease
|
Albers-Schonberg Disease
|
|
Osteopetroses
|
Marble Bones
|
|
Osteopetrosis And Related Disorders
|
Congenital Osteopetrosis
|
|
Marble Bone
|
Albers-Schoenberg Disease
|
|
Albers-Schonberg Osteopetrosis
|
Osteosclerosis Fragilis
|
|
Ivory Bones
|
|
|
| Angiomyolipoma |
|
|
| Melanoma |
|
Malignant Melanoma
|
Cutaneous Melanoma
|
|
Naevocarcinoma
|
Malignant Melanomas
|
|
|
| Renal Cell Carcinoma, Papillary, 1 |
|
Papillary Renal Cell Carcinoma
|
Hereditary Papillary Renal Cell Carcinoma
|
|
Papillary Renal Cell Carcinoma, Sporadic
|
Papillary Renal Cell Adenocarcinoma
|
|
RCCP
|
RCCP1
|
|
Renal Cell Carcinoma, Papillary
|
Renal Cell Carcinoma, Papillary, 1, Familial And Somatic
|
|
Chromophil Carcinoma Of Kidney
|
Papillary Kidney Carcinoma
|
|
Sporadic Papillary Renal Cell Carcinoma
|
Chromophil Renal Cell Carcinoma
|
|
Papillary Renal Carcinoma, Malignant -
|
Papillary Renal Cell Carcinoma, Bilateral -
|
|
Papillary Renal Cell Carcinoma, Familial -
|
Papillary Renal Cell Carcinoma, Multiple -
|
|
Papillary Renal Cell Carcinoma, Sporadic -
|
Renal Adenocarcinoma
|
|
Chromophil Rcc
|
Hprcc
|
|
Renal Cell Carcinoma Papillary
|
Chromophilic Renal Cell Carcinoma
|
|
Prcc
|
Carcinoma, Renal Cell, Papillary, Type 1
|
|
Type 1 Papillary Renal Cell Carcinoma
|
Renal Cell Carcinoma
|
|
Hereditary Papillary Renal Carcinoma
|
|
|
| Pigmentation Disease |
|
Pigmentation Disorders
|
Skin Pigmentation Disorder
|
|
|
| Melanoma, Cutaneous Malignant 1 |
|
Familial Melanoma
|
Melanoma, Cutaneous Malignant, Susceptibility To, 1
|
|
Melanoma, Malignant
|
CMM1
|
|
Melanoma, Cutaneous Malignant
|
Cmm
|
|
Familial Atypical Mole-Malignant Melanoma Syndrome
|
Fammm
|
|
Melanoma, Familial
|
Mlm
|
|
Dysplastic Nevus Syndrome, Hereditary
|
Dns
|
|
B-K Mole Syndrome
|
Melanoma, Cutaneous Malignant, 1
|
|
Malignant Melanoma, Cutaneous
|
Melanoma, Cutaneous, Malignant, Susceptibility To, Type 1
|
|
Dysplastic Nevus Syndrome
|
Cutaneous Melanoma
|
|
Familial Atypical Mole Melanoma Syndrome
|
Hereditary Melanoma
|
|
|
| Neurofibroma |
|
Neurofibromas
|
Neurofibromatoses
|
|
Nerve Sheath Tumors
|
|
|
| Fibrous Histiocytoma |
|
Benign Fibrous Histiocytoma
|
Histiocytoma, Benign Fibrous
|
|
Fibroxanthoma
|
Histiocytoma Fibrous
|
|
|
| Melanoma In Congenital Melanocytic Nevus |
|
Malignant Melanoma In Congenital Melanocytic Nevus
|
Melanocytic Nevi
|
|
Nevi Melanocytic
|
|
|
| Sensorineural Hearing Loss |
|
Sensory Hearing Loss
|
Sensorineural Deafness
|
|
Sensorineural Hearing Loss Disorder
|
Hearing Loss, Sensorineural
|
|
Central Hearing Loss
|
High Frequency Deafness
|
|
High Frequency Hearing Loss
|
High-Frequency Hearing Loss
|
|
Perceptive Deafness
|
Perceptive Hearing Loss
|
|
Perceptive Hearing Loss Or Deafness
|
Hearing Loss Sensorineural
|
|
Deafness Sensorineural
|
Hearing Loss High-Frequency
|
|
Hearing Loss, Central
|
Hearing Loss, High-Frequency
|
|
|
| Albinism-Deafness Syndrome |
|
Alds
|
Albinism Deafness Syndrome
|
|
ADFN
|
Albinism-Hearing Loss Syndrome
|
|
|
| Pycnodysostosis |
|
Pyknodysostosis
|
PKND
|
|
Pycd
|
Toulouse-Lautrec Syndrome
|
|
|
| Waardenburg Syndrome, Type 3 |
|
Waardenburg Syndrome Type 3
|
Klein-Waardenburg Syndrome
|
|
WS3
|
Waardenburg Syndrome With Upper Limb Anomalies
|
|
Waardenburg Syndrome Type Iii
|
Waardenburg Syndrome, Type Iii
|
|
White Forelock Syndrome With Multiple Congenital Malformations
|
Waardenburg Syndrome With Limb Anomalies
|
|
Waardenburg Syndrome 3
|
White Forelock With Malformations
|
|
Klein'S Syndrome
|
|
|
| Albinism |
|
|
| Piebald Trait |
|
Piebaldism
|
PBT
|
|
Partial Albinism
|
Albinoidism, Oculocutaneous, Autosomal Dominant
|
|
|
| Autosomal Dominant Intellectual Developmental Disorder 19 |
|
Autosomal Dominant Non-Syndromic Intellectual Disability 19
|
Autosomal Dominant Mental Retardation 19
|
|
Mrd19
|
|
|
| Hereditary Breast Ovarian Cancer Syndrome |
|
Hereditary Breast And Ovarian Cancer Syndrome
|
Brca1- And Brca2-Associated Hereditary Breast And Ovarian Cancer
|
|
Breast And/Or Ovarian Cancer
|
Breast And Ovarian Cancer Syndrome
|
|
Hboc Syndrome
|
Hereditary Breast And Ovarian Cancer
|
|
Brca1- Brca2-Associated Hboc
|
|
|
| Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 |
|
Vitiligo
|
VAMAS1
|
|
Slev1
|
Vtlg
|
|
Systemic Lupus Erythematosus, Vitiligo-Related
|
Vitiligo-Associated Multiple Autoimmune Disease 1
|
|
Systemic Lupus Erythematosus Vitiligo-Related
|
|
|
| Mastocytosis |
|
Mast Cell Disease
|
Mast Cell Hyperplasia
|
|
Urticaria Pigmentosa
|
Malignant Mastocytoma
|
|
Malignant Mast Cell Tumours
|
Malignant Mastocytosis
|
|
|
| Ocular Albinism |
|
Albinism, Ocular
|
Oa
|
|
Xloa
|
Albinism Ocular
|
|
|
| Nodular Malignant Melanoma |
|
|
| Malignant Spindle Cell Melanoma |
|
Spindle Cell Melanoma
|
Desmoplastic Melanoma
|
|
Spindle Cell Malignant Melanoma
|
Spitzoid Malignant Melanoma
|
|
|
| Epithelioid Cell Melanoma |
|
|
| Perivascular Epithelioid Cell Tumor |
|
Pecoma
|
Perivascular Epithelioid Cell Neoplasms
|
|
Neoplasm With Perivascular Epithelioid Cell Differentiation
|
|
|
| Pigmented Basal Cell Carcinoma |
|
Skin Pigmented Basal Cell Carcinoma
|
|
|
| Melanoma, Uveal |
|
Uveal Melanoma
|
Choroidal Melanoma
|
|
Melanoma Of Uvea
|
Iris Melanoma
|
|
Malignant Melanoma Of Choroid
|
Malignant Melanoma Of Iris
|
|
|
| Pendred Syndrome |
|
Goiter-Deafness Syndrome
|
Deafness With Goiter
|
|
PDS
|
Thyroid Dyshormonogenesis 2b
|
|
Tdh2b
|
Autosomal Recessive Sensorineural Hearing Impairment And Goiter
|
|
Pendred'S Syndrome
|
Thyroid Hormonogenesis, Genetic Defect In, 2b
|
|
Hypothyroidism, Congenital, Due To Dyshormonogenesis, 2b
|
Congenital Hypothyroidism Due To Dyshormonogenesis 2b
|
|
Genetic Defect In Thyroid Hormonogenesis 2b
|
Autosomal Recessive Sensorineural Hearing Impairment, Enlarged Vestibular Aqueduct, And Goiter
|
|
Goiter-Hearing Loss Syndrome
|
Goitre-Deafness Syndrome
|
|
Goitre Deafness
|
|
|
| Waardenburg Syndrome, Type 2c |
|
Waardenburg Syndrome Type 2c
|
WS2C
|
|
Waardenburg Syndrome, Type Iic
|
Waardenburg Syndrome Type Iic
|
|
|
| Oculocutaneous Albinism |
|
Albinism, Oculocutaneous
|
Oca
|
|
Albinism Oculocutaneous
|
Oca - [Oculocutaneous Albinism]
|
|
|
| Waardenburg Syndrome, Type 4c |
|
Waardenburg Syndrome Type 4c
|
WS4C
|
|
Waardenburg Syndrome Type Ivc
|
Waardenburg Syndrome With Hirschsprung Disease Type 4c
|
|
Waardenburg Syndrome With Hirschsprung Disease, Type 4c
|
Waardenburg Syndrome, Type Ivc
|
|
Waardenburg Syndrome 4c
|
Hirschsprung Disease With Pigmentary Anomaly
|
|
Shah-Waardenburg Syndrome
|
Waardenburg-Shah Syndrome
|
|
Waardenburg Syndrome, Type 4a
|
|
|
| Waardenburg Syndrome, Type 2b |
|
Waardenburg Syndrome Type 2b
|
WS2B
|
|
Waardenburg Syndrome, Type Iib
|
Waardenburg Syndrome Type Iib
|
|
|
| Gallbladder Melanoma |
|
Malignant Melanoma Of Gallbladder
|
|
|
| Acral Lentiginous Melanoma |
|
Acral Lentiginous Melanoma, Malignant
|
Malignant Acral Lentiginous Melanoma
|
|
Alm
|
Acral Lentiginous Malignant Melanoma Of Skin
|
|
Palmar/Plantar Melanoma
|
Subungual Melanoma
|
|
Acral Lentiginous Malignant Melanoma
|
|
|
| Perivascular Tumor |
|
Malignant Perivascular Cancer
|
|
|
| Malignant Peripheral Nerve Sheath Tumor |
|
Mpnst
|
Malignant Neurilemmoma
|
|
Neurofibrosarcoma
|
Malignant Neurofibroma
|
|
Malignant Schwannoma
|
Neurogenic Sarcoma
|
|
Schwannoma, Malignant
|
Malignant Neoplasm Of The Peripheral Nerve Sheath
|
|
Malignant Peripheral Nerve Sheath Tumors
|
|
|
| Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease |
|
Pcwh Syndrome
|
PCWH
|
|
Neurologic Waardenburg-Shah Syndrome
|
Waardenburg-Shah Syndrome, Neurologic Variant
|
|
Peripheral Demyelinating Neuropathy-Central Dysmyelinating Leukodystrophy-Hirschsprung Disease-Waardenburg Syndrome
|
Peripheral Demyelinating Neuropathy-Central Dysmyelinating Leukodystrophy-Waardenburg Syndrome-Hirschsprung Disease
|
|
Ws4 Plus
|
Peripheral Demyelinating Neuropathy, Central Dysmyelinating Leukodystrophy, Waardenburg Syndrome And Hirschsprung Disease
|
|
Waardenburg-Shah Syndrome Neurologic Variant
|
|
|
| Albinism, Ocular, With Late-Onset Sensorineural Deafness |
|
Ocular Albinism With Sensorineural Deafness
|
OASD
|
|
Deafness And Ocular Albinism
|
Ocular Albinism With Late-Onset Sensorineural Deafness
|
|
Albinism, Ocular, With Sensorineural Deafness
|
Autosomal Recessive Waardenburg Syndrome Type 2 With Ocular Albinism
|
|
Digenic Waardenburg Syndrome/Albinism
|
Digenic Waardenburg Syndrome/Ocular Albinism
|
|
Ws2-Oa
|
Albinism Ocular Late Onset Sensorineural Deafness
|
|
Ocular Albinism With Late-Onset Sensorineural Hearing Loss
|
Waardenburg Syndrome/Ocular Albinism, Digenic
|
|
Waardenburg Syndrome/Albinism, Digenic
|
Ocular Albinism And Sensorineural Deafness
|
|
|
| Ochronosis |
|
|
| Mucosal Melanoma |
|
|
| Waardenburg Syndrome, Type 2d |
|
Waardenburg Syndrome Type 2d
|
WS2D
|
|
Waardenburg Syndrome, Type Iid
|
Waardenburg Syndrome Type Iid
|
|
Waardenburg Syndrome 2d
|
|
|
| Amelanotic Melanoma |
|
Melanoma, Amelanotic
|
Melanoma Amelanotic
|
|
Amelanotic Skin Melanoma
|
|
|
| Dowling-Degos Disease 1 |
|
Reticular Pigment Anomaly Of Flexures
|
DDD1
|
|
Ddd
|
Hyperpigmentation
|
|
Dowling-Degos Disease
|
|
|
| Meningeal Melanoma |
|
Melanoma Of The Leptomeninges
|
Leptomeningeal Melanoma
|
|
|
| Malignant Leptomeningeal Tumor |
|
Malignant Leptomeningeal Tumour
|
Malignant Tumor Of Leptomeninges
|
|
Malignant Tumour Of Leptomeninges
|
Malignant Leptomeningeal Neoplasm
|
|
|
| Childhood Kidney Cell Carcinoma |
|
Pediatric Renal Cell Carcinoma
|
Childhood Renal Cell Carcinoma
|
|
|
| Cowden Syndrome 4 |
|
CWS4
|
Cowden Syndrome, Type 4
|
|
|
| Uterus Perivascular Epithelioid Cell Tumor |
|
|
| Neurilemmoma |
|
Schwannoma
|
Benign Schwannoma
|
|
Neurilemoma
|
Peripheral Fibroblastoma
|
|
Psammomatous Schwannoma
|
Neurolemmoma
|
|
Schwannomas
|
|
|
| Epithelioid Type Angiomyolipoma |
|
Epithelioid Angiomyolipoma
|
|
|
| Paraganglioma |
|
Chemodectoma
|
Glomus Body Tumor
|
|
Paragangliomas
|
Carotid Body Paraganglioma
|
|
Extra-Adrenal Paraganglioma
|
|
|
| Cutaneous Ganglioneuroma |
|
|
| Benign Giant Cell Tumor |
|
|
| Alveolar Soft Part Sarcoma |
|
ASPS
|
Alveolar Soft-Part Sarcoma
|
|
Sarcoma, Alveolar Soft Part
|
Alveolar Soft Tissue Sarcoma
|
|
Sarcoma Alveolar Soft Part
|
Adult Alveolar Soft-Part Sarcoma
|
|
Childhood Alveolar Soft-Part Sarcoma
|
|
|
| Macular Degeneration, Age-Related, 7 |
|
Age Related Macular Degeneration 7
|
ARMD7
|
|
Macular Degeneration, Age-Related, Neovascular Type
|
Susceptibility To Neovascular Type Of Age-Related Macular Degeneration
|
|
Macular Degeneration, Age-Related, Type 7
|
|
|
| Hirschsprung Disease 1 |
|
Hirschsprung Disease
|
Aganglionic Megacolon
|
|
Hscr
|
Hirschsprung'S Disease
|
|
Congenital Megacolon
|
Congenital Intestinal Aganglionosis
|
|
Colonic Aganglionosis
|
Hirschsprung Disease, Susceptibility To, 1
|
|
Hirschsprung Disease, Protection Against
|
HSCR1
|
|
Mgc
|
Pelvirectal Achalasia
|
|
Total Intestinal Aganglionosis
|
Megacolon, Aganglionic
|
|
Macrocolon
|
Hscr 1
|
|
Hirschsprung Disease Type 1
|
Hirschsprung Disease, Type 1
|
|
Congenital Dilatation Of Colon
|
Aganglionosis
|
|
Congenital Aganglionic Megacolon
|
Aganglionosis Of Colon
|
|
Bowel Aganglionosis
|
Colon Aganglionosis
|
|
Hirschsprung Megacolon
|
|
|
| Large Congenital Melanocytic Nevus |
|
Giant Pigmented Hairy Nevus
|
Giant Congenital Melanocytic Nevus
|
|
Gmn
|
Congenital Pigmented Nevus
|
|
Lcmn
|
Gphn
|
|
Giant Congenital Nevus
|
Bathing Trunk Nevus
|
|
Congenital Giant Pigmented Nevus
|
Congenital Hairy Nevus
|
|
Giant Hairy Nevus
|
Giant Pigmented Nevus
|
|
Congenital Giant Pigmented Nevus Of Skin
|
Congenital Melanocytic Nevus Syndrome
|
|
Giant Congenital Melanocytic Nevi
|
Giant Congenital Pigmented Nevus
|
|
Melanocytic Nevus Syndrome, Congenital
|
|
|
| Skin Carcinoma |
|
Skin Cancer
|
Carcinoma Of Skin
|
|
Ca - Skin Cancer
|
Cancer Of Skin
|
|
Malignant Neoplasm Of Skin
|
Melanoma And Non-Melanoma Skin Cancer
|
|
Skin Cancers
|
Cancer, Skin
|
|
|
| Hepatic Angiomyolipoma |
|
|
| Cutaneous Fibrous Histiocytoma |
|
Dermatofibroma
|
Fibrohistiocytic Tumor
|
|
Benign Cutaneous Fibrous Histiocytoma
|
Fibrous Histiocytoma Of Skin
|
|
Fibrous Xanthoma Of Skin
|
Pleomorphic Fibroma
|
|
Sclerosing Angioma
|
Sclerosing Angioma Of Skin
|
|
Fibrous Histiocytoma
|
|
|
| Kidney Angiomyolipoma |
|
Angiomyolipoma Of Kidney
|
Renal Angiomyolipoma
|
|
|
| Vascular Cancer |
|
Blood Vessel Tumors
|
Malignant Vascular Neoplasm
|
|
Renal Vein Leiomyosarcoma
|
Vascular Neoplasms
|
|
Blood Vessel Neoplasm
|
Blood Vessel Tumor
|
|
Blood Vessel Tumour Disorder
|
Haemangiomatous Tumour
|
|
Leiomyosarcoma Of The Renal Vein
|
Malignant Great Vessel Tumor
|
|
Malignant Tumor Of Pulmonary Artery
|
Malignant Tumor Of Pulmonary Vein
|
|
Malignant Vascular Tumor
|
Neoplasm Of Great Vessel
|
|
Pulmonary Artery Malignant Neoplasm
|
Pulmonary Vein Malignant Neoplasm
|
|
Vascular Tissue Neoplasm
|
Vascular Tumors
|
|
Blood Vessel Cancer
|
Neoplasms, Vascular Tissue
|
|
Malignant Neoplasm Of Great Vessels
|
|
|
| Keratosis, Seborrheic |
|
Seborrheic Keratosis
|
Keratosis, Seborrheic, Somatic
|
|
Basal Cell Papilloma
|
Keratosis Seborrheica
|
|
KERSEB
|
|
|
| Renal Cell Carcinoma, Nonpapillary |
|
Renal Cell Carcinoma
|
RCC
|
|
Nonpapillary Renal Cell Carcinoma
|
Clear Cell Renal Cell Carcinoma
|
|
Hypernephroma
|
Adenocarcinoma Of Kidney
|
|
Renal Carcinoma, Chromophobe, Somatic
|
Clear Cell Carcinoma Of Kidney
|
|
Clear-Cell Metastatic Renal Cell Carcinoma
|
Clear Cell Renal Carcinoma
|
|
Renal Cell Carcinoma, Somatic
|
Conventional Renal Cell Carcinoma
|
|
Conventional Renal Cell Carcinoma
|
Renal Clear Cell Carcinoma
|
|
Ccrcc
|
Hereditary Clear Cell Renal Cell Carcinoma
|
|
Carcinoma, Renal Cell
|
Renal Cell Carcinoma, Clear Cell, Somatic
|
|
Renal Cell Carcinoma, Clear Cell
|
Clear Cell Kidney Carcinoma
|
|
Clear Cell Rcc
|
Cystic-Multilocular Variant
|
|
Clear Cell Renal Cell Adenocarcinoma
|
Hereditary Clear Cell Renal Cell Adenocarcinoma
|
|
Common Renal Cell Carcinoma
|
Crcc
|
|
Renal Cell Carcinoma Non-Papillary
|
Carcinoma Renal Cell
|
|
Renal Cell Cancer
|
Carcinoma, Renal Cell, Nonpapillary
|
|
|
| Skin Melanoma |
|
Cutaneous Melanoma
|
Malignant Ear Melanoma
|
|
Malignant Lip Melanoma
|
Malignant Lower Limb Melanoma
|
|
Malignant Melanoma Of Ear And/Or External Auricular Canal
|
Malignant Melanoma Of Skin Of Lower Limb
|
|
Malignant Melanoma Of Skin Of Trunk Except Scrotum
|
Malignant Melanoma Of Skin Of Upper Limb
|
|
Malignant Neck Melanoma
|
Malignant Scalp Melanoma
|
|
Malignant Trunk Melanoma
|
Malignant Upper Limb Melanoma
|
|
Melanoma, Cutaneous Malignant
|
Melanoma
|
|
Malignant Melanoma Of Skin
|
Melanoma Nos
|
|
Malignant Mole, Meaning Melanoma Of Unspecified Site
|
Melanoma Of Unspecified Site
|
|
Cutaneous Malignant Melanoma
|
Mm - [Malignant Melanoma]
|
|
|
| Spinal Cord Melanoma |
|
Melanoma Of The Spinal Cord
|
|
|
| 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
|
|
|
| Cervix Melanoma |
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Ocular Melanoma |
|
Intraocular Melanoma
|
Uveal Melanoma
|
|
Eye Melanoma
|
Melanoma Of Eye
|
|
Melanoma Of The Uvea
|
Malignant Melanoma Of Eye
|
|
|
| Skin Disease |
|
Skin Diseases
|
Genodermatosis
|
|
Abnormality Of The Skin
|
Skin Diseases, Genetic
|
|
Skin And Subcutaneous Tissue Disease
|
Dermatologic Disorders
|
|
|
| Uveal Disease |
|
|
| Coloboma Of Macula |
|
Coloboma
|
Congenital Ocular Coloboma
|
|
Microphthalmia, Isolated, With Coloboma
|
Agenesis Of Macula
|
|
Hereditary Macular Coloboma
|
Ocular Coloboma
|
|
Coloboma Of Eye
|
Macular Coloboma
|
|
Uveoretinal Coloboma
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
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
|
|
|
