| Diseases |
Alias |
|
| Oculodentodigital Dysplasia |
|
Odd Syndrome
|
ODDD
|
|
Oculodentoosseous Dysplasia
|
Oculodentodigital Syndrome
|
|
Odod
|
Oculo-Dento-Digital Dysplasia
|
|
Oculo-Dento-Digital Syndrome
|
Oculo-Dento-Osseous Dysplasia
|
|
Osseous-Oculo-Dental Dysplasia
|
Meyer-Schwickerath Syndrome
|
|
Oddd Syndrome
|
Oculo Dento Digital Dysplasia
|
|
Odds
|
Oculodentodigital Dysplasia Syndrome
|
|
|
| Syndactyly, Type Iii |
|
Syndactyly Type 3
|
SDTY3
|
|
Ring And Little Finger Syndactyly
|
Syndactyly Of Fingers Iv And V
|
|
Syndactyly Of Fingers 4 And 5
|
Ringand Little Finger Syndactyly
|
|
Syndactyly Of Fingers Four And Five
|
Syndactyly Of The Ring And Little Finger
|
|
Sd3
|
Syndactyly 3
|
|
Syndactyly Type Iii
|
4-5 Finger Syndactyly
|
|
Syndactyly, Type 3
|
|
|
| Palmoplantar Keratoderma And Congenital Alopecia 1 |
|
Autosomal Dominant Palmoplantar Keratoderma And Congenital Alopecia
|
PPKCA1
|
|
Keratoderma-Hypotrichosis-Leukonychia Totalis Syndrome
|
Autosomal Dominant Palmoplantar Hyperkeratosis And Congenital Alopecia
|
|
Palmoplantar Keratoderma And Congenital Alopecia, Stevanovic Type
|
Ppk-Ca, Stevanovic Type
|
|
Ppkca, Stevanovic Type
|
Palmoplantar Keratoderma With Congenital Alopecia
|
|
Ppkca Stevanovic Type
|
Alopecia Congenita With Hyperkeratosis Of The Palms And Soles
|
|
Alopecia Congenita Keratosis Palmoplantaris
|
Keratoderma, Palmoplantar, With Congenital Alopecia, Type 1
|
|
|
| Craniometaphyseal Dysplasia, Autosomal Recessive |
|
CMDR
|
Autosomal Recessive Craniometaphyseal Dysplasia
|
|
Craniometaphyseal Dysplasia, Autosomal Recessive Type
|
Dysplasia, Craniometaphyseal, Autosomal Recessive
|
|
|
| Erythrokeratodermia Variabilis Et Progressiva 3 |
|
|
| Oculodentodigital Dysplasia, Autosomal Recessive |
|
Oddd, Autosomal Recessive
|
Oculodentoosseous Dysplasia, Autosomal Recessive
|
|
Odod, Autosomal Recessive
|
ODDD-AR
|
|
Autosomal Recessive Oculodentoosseous Dysplasia
|
Autosomal Recessive Oddd
|
|
Autosomal Recessive Odd Syndrome
|
Autosomal Recessive Odod
|
|
|
| Atrioventricular Septal Defect 3 |
|
AVSD3
|
Septal Defect, Atrioventricular, Type 3
|
|
|
| Hypoplastic Left Heart Syndrome 1 |
|
HLHS1
|
Hlhs
|
|
Hypoplastic Left Heart Syndrome
|
|
|
| Hallermann-Streiff Syndrome |
|
Francois Dyscephalic Syndrome
|
HSS
|
|
Hallermann'S Syndrome
|
Oculomandibulofacial Syndrome
|
|
Hallerman - Streiff Syndrome
|
François Dyscephalic Syndrome
|
|
Hallermann Streiff Francois Syndrome
|
Hallermann Streiff Syndrome
|
|
|
| Syndactyly, Type V |
|
Syndactyly Type 5
|
SDTY5
|
|
Syndactyly With Metacarpal And Metatarsal Fusion
|
Syndactyly With Associated Metacarpal And Metatarsal Fusion
|
|
Postaxial Syndactyly With Metacarpal Synostosis
|
Sd5
|
|
Syndactyly 5
|
Syndactyly Type V
|
|
|
| Erythrokeratodermia Variabilis Et Progressiva 1 |
|
Erythrokeratodermia Variabilis
|
Erythrokeratodermia Variabilis Et Progressiva
|
|
Greither Disease
|
Ekv
|
|
Ekvp
|
PSEK
|
|
Erythrokeratodermia Variabilis With Erythema Gyratum Repens
|
Keratosis Palmoplantaris Transgrediens Et Progrediens
|
|
Transgrediens Et Progrediens Palmoplantar Keratoderma
|
EKVP1
|
|
Erythrokeratodermia, Progressive Symmetric
|
Erythrokeratodermia Figurata, Congenital Familial, In Plaques
|
|
Keratoderma Palmoplantaris Transgrediens
|
Keratosis Extremitatum Hereditaria Progrediens
|
|
Erythrokeratodermia Variabilis, Mendes Da Costa Type
|
Progressive Symmetric Erythrokeratodermia
|
|
Erythrokeratodermia Figurata Variabilis
|
Greither'S Disease
|
|
Ekv-P
|
Erythrokeratodermia Variabilis Of Mendes Da Costa
|
|
Progressive Symmetrical Erythrokeratoderma Of Gottron
|
Progressive Diffuse Ppk
|
|
Progressive Diffuse Palmoplantar Keratoderma
|
Transgrediens Et Progrediens Ppk
|
|
Darier-Gottron Disease
|
Erythrokeratodermia Progressiva Symmetrica
|
|
Progressive Symmetric Erythrokeratodermia, Gottron Type
|
Congenital Familial Erythrokeratodermia Figurata In Plaques
|
|
Erythrokeratodermia Progressive Symmetric
|
Erythrokeratodermia Variabilis Mendes Da Costa Type
|
|
|
| Craniometaphyseal Dysplasia, Autosomal Dominant |
|
Craniometaphyseal Dysplasia
|
CMDD
|
|
Cmdj
|
Cmd
|
|
Autosomal Dominant Craniometaphyseal Dysplasia
|
Craniometaphyseal Dysplasia, Jackson Type
|
|
Craniometaphyseal Dysplasia Jackson Type
|
Autosomal Recessive Craniometaphyseal Dysplasia
|
|
Cmdr
|
Dysplasia, Craniometaphyseal, Autosomal Dominant
|
|
Craniometaphyseal Dysplasia, Autosomal Recessive Type
|
|
|
| Hypoplastic Left Heart Syndrome |
|
Hlhs
|
Heart, Hypoplastic Left, Syndrome
|
|
Hypoplasia Of The Left Heart
|
Left Heart Hypoplasia Syndrome
|
|
Hlhs - [Hypoplastic Left Heart Syndrome]
|
Hypoplasia Of Aortic Valve, In Hypoplastic Left Heart Syndrome
|
|
Atresia Of Mitral Valve, In Hypoplastic Left Heart Syndrome
|
Atresia Or Marked Hypoplasia Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle
|
|
Atresia Or Marked Hypoplasia, Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle With Mitral Valve Atresia
|
Aortic Valve Atresia, In Hypoplastic Left Heart Syndrome
|
|
Ascending Aorta Hypoplasia, In Hypoplastic Left Heart Syndrome
|
|
|
| Hyperostosis |
|
Hypertrophy Of Bone
|
Bone Hypertrophy
|
|
Bone Thickening
|
Periosteum Thickening
|
|
|
| Arrhythmogenic Right Ventricular Cardiomyopathy |
|
Arrhythmogenic Right Ventricular Dysplasia
|
Arvc
|
|
Arvd
|
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
|
|
Arvc Cardiomyopathy
|
Arrhythmogenic Right Ventricular Cardiomyopathy-Dysplasia
|
|
Arvd/C
|
Right Ventricular Dysplasia, Arrhythmogenic
|
|
Ventricular Dysplasia, Right, Arrhythmogenic
|
Cardiomyopathy, Ventricular, Right, Arrhythmogenic
|
|
Dysplasia, Arrhythmogenic Right Ventricular
|
|
|
| Skin Atrophy |
|
Atrophic Condition Of Skin
|
Atrophoderma
|
|
Atrophy - Skin
|
|
|
| Hypotrichosis |
|
|
| Atrioventricular Septal Defect |
|
AVSD
|
Atrioventricular Canal Defect
|
|
Avcd
|
Endocardial Cushion Defect
|
|
Ecd
|
Avc Defect
|
|
Atrioventricular Septal Defect, Susceptibility To, 1
|
Atrioventricular Septal Defect 1
|
|
Endocardial Cushion Defects
|
Septal Defect, Atrioventricular
|
|
Atrioventricular Defect With Atrial Shunting Only
|
Incomplete Atrioventricular Septal Defect With Isolated Atrial Component
|
|
Incomplete Atrioventricular Canal Defect With Isolated Atrial Component
|
Primum Atrial Septal Defect
|
|
Partial Atrioventricular Canal Defect With Isolated Atrial Component
|
Partial Atrioventricular Septal Defect, Ostium Primum Type
|
|
Ostium Primum Atrial Septal Defect
|
Partial Atrioventricular Canal Defect
|
|
Partial Atrioventricular Septal Defect
|
Atrial Septum Primum Defect
|
|
Atrioventricular Canal Defect With Isolated Ventricular Component
|
Atrioventricular Canal Defect With Isolated Ventricular Communication
|
|
Atrioventricular Septal Defect With Isolated Ventricular Component
|
Atrioventricular Septal Defect With Atrial Shunting And Restrictive Ventricular Shunting
|
|
Intermediate Atrioventricular Canal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valve
|
Transitional Atrioventricular Septal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valves
|
|
Atrioventricular Canal Defect Associated With A Restrictive Ventricular Septal Defect
|
Intermediate Atrioventricular Canal Defect
|
|
Intermediate Atrioventricular Septal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valvar Orifices
|
Intermediate Atrioventricular Septal Defect
|
|
Transitional Atrioventricular Canal Defect
|
Transitional Atrioventricular Septal Defect
|
|
Complete Atrioventricular Canal With Atrial And Ventricular Components
|
Complete Atrioventricular Canal Defect
|
|
Complete Atrioventricular Septal Defect
|
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Heart Malformation
|
|
Congenital Anomaly Of Heart
|
Heart Defect
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Chromosome 2q35 Duplication Syndrome |
|
Syndactyly
|
Syndactyly Type 1
|
|
Sdty1
|
Zygodactyly
|
|
Syndactyly, Type I
|
Sd1
|
|
Syndactyly, Type 1, With Or Without Craniosynostosis
|
Symphalangism
|
|
Non-Syndromic Syndactyly
|
Symphalangy
|
|
Webbing Of Digits
|
Syndactyly, Type 1
|
|
|
| Lung Giant Cell Carcinoma |
|
Carcinoma, Giant Cell
|
Giant Cell Carcinoma
|
|
Giant Cell Lung Carcinoma
|
Carcinoma Giant Cell
|
|
Giant Cell Carcinoma Of Lung
|
|
|
| Atrial Fibrillation |
|
A-Fib
|
Fibrillation, Atrial
|
|
Af - [Atrial Fibrillation]
|
Rapid Atrial Fibrillation
|
|
A Fib - [Atrial Fibrillation]
|
|
|
| Palmoplantar Keratosis |
|
Palmoplantar Keratoderma
|
Keratosis Palmaris Et Plantaris
|
|
Palmo-Plantar Keratodermas
|
Keratoderma, Palmoplantar
|
|
Keratoderma Palmoplantar
|
Keratoderma, Palmoplantar, Diffuse
|
|
Hyperkeratosis Of Palms And Soles
|
Palmoplantar Hyperkeratosis
|
|
|
| Keratosis |
|
Actinic Keratosis
|
Hyperkeratosis
|
|
|
| Seminoma |
|
|
| Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb |
|
Autosomal Recessive Isolated Neurosensory Deafness Type Dfnb
|
Autosomal Recessive Isolated Neurosensory Hearing Loss Type Dfnb
|
|
Autosomal Recessive Isolated Sensorineural Deafness Type Dfnb
|
Autosomal Recessive Isolated Sensorineural Hearing Loss Type Dfnb
|
|
Autosomal Recessive Non-Syndromic Neurosensory Deafness Type Dfnb
|
Autosomal Recessive Non-Syndromic Neurosensory Hearing Loss Type Dfnb
|
|
Autosomal Recessive Non-Syndromic Sensorineural Hearing Loss Type Dfnb
|
|
|
| Tetralogy Of Fallot |
|
TOF
|
Fallot Tetralogy
|
|
Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle
|
Tetrad Of Fallot
|
|
Fallot Tetrad
|
Fallot Disease
|
|
Fallot Complex
|
Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy
|
|
Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle
|
Interventricular Septal Defect, In Tetralogy Of Fallot
|
|
Ventricular Septal Defect With Obstructed Right Ventricular Outflow
|
Tof - [Tetralogy Of Fallot]
|
|
Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]
|
Pulmonary Atresia, Ventricular Septal Defect And Mapcas
|
|
Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
|
|
|
| Ischemia |
|
|
| Bart-Pumphrey Syndrome |
|
Knuckle Pads, Leukonychia, And Sensorineural Deafness
|
BAPS
|
|
Knuckle Pads, Leuconychia And Sensorineural Deafness
|
Knuckle Pads-Leukonychia-Sensorineural Deafness-Palmoplantar Hyperkeratosis Syndrome
|
|
Knuckle Pads-Leukonychia-Sensorineural Deafness-Palmoplantar Keratoderma Syndrome
|
Knuckle Pads, Deafness And Leukonychia Syndrome
|
|
Knuckle Pads, Deafness, And Leukonychia Syndrome
|
Knuckle Pads-Leukonychia-Sensorineural Hearing Loss-Palmoplantar Hyperkeratosis Syndrome
|
|
Knuckle Pads-Leukonychia-Sensorineural Hearing Loss-Palmoplantar Keratoderma Syndrome
|
|
|
| Skin Disease |
|
Skin Diseases
|
Genodermatosis
|
|
Abnormality Of The Skin
|
Skin Diseases, Genetic
|
|
Skin And Subcutaneous Tissue Disease
|
Dermatologic Disorders
|
|
|
| Leiomyoma |
|
Leiomyomatous Neoplasm
|
Leiomyomatous Tumor
|
|
Leiomyomas
|
Fibroid Tumor
|
|
Uterine Fibroids
|
|
|
| Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant |
|
Kid Syndrome
|
Keratitis-Ichthyosis-Deafness Syndrome
|
|
Senter Syndrome
|
KIDAD
|
|
Kid Syndrome, Autosomal Dominant
|
Autosomal Dominant Keratitis-Ichthyosis-Deafness Syndrome
|
|
Ichthyosis Hystrix Rheydt Type
|
Kid/Hid Syndrome
|
|
Keratitis-Ichthyosis-Deafness/Hystrix-Like Ichthyosis-Deafness Syndrome
|
Keratitis Ichthyosis And Deafness Syndrome
|
|
Autosomal Dominant Kid Syndrome
|
Keratitis, Ichthyosis, And Deafness Syndrome
|
|
Ichthyosiform Erythroderma, Corneal Involvement, And Deafness
|
Keratitis, Ichthyosis, And Deafness
|
|
Keratitis-Ichthyosis-Hearing Loss/Hystrix-Like Ichthyosis-Hearing Loss Syndrome
|
|
|
| Temporal Lobe Epilepsy |
|
Epilepsy, Temporal Lobe
|
Epilepsy Temporal Lobe
|
|
|
| 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
|
|
|
| Clouston Syndrome |
|
Ectodermal Dysplasia 2, Clouston Type
|
Hidrotic Ectodermal Dysplasia
|
|
ECTD2
|
Clouston'S Hidrotic Ectodermal Dysplasia
|
|
Hidrotic Ectodermal Dysplasia Syndrome
|
Clouston Hidrotic Ectodermal Dysplasia
|
|
Clouston'S Syndrome
|
Ed2
|
|
Ectodermal Dysplasia, Hidrotic
|
Hed2
|
|
Ectodermal Dysplasia
|
Ectodermal Dysplasia, Hidrotic, Autosomal Dominant
|
|
Ectodermal Dysplasia, Hidrotic, 2, Formerly
|
Hed2, Formerly
|
|
Autosomal Dominant Hidrotic Ectodermal Dysplasia
|
Hed
|
|
Hidrotic Ectodermal Dysplasia, Autosomal Dominant
|
Hidrotic Ectodermal Dysplasia 2
|
|
Ectodermal Dysplasia 2 Hidrotic
|
Ectodermal Dysplasia Hidrotic Autosomal Dominant
|
|
Dysplasia, Ectodermal, Hidrotic
|
|
|
| Keratoderma, Palmoplantar, With Deafness |
|
Palmoplantar Keratoderma-Deafness Syndrome
|
Palmoplantar Keratoderma With Deafness
|
|
Palmoplantar Hyperkeratosis-Deafness Syndrome
|
Palmoplantar Hyperkeratosis-Hearing Loss Syndrome
|
|
Palmoplantar Keratoderma-Hearing Loss Syndrome
|
Ppk-Deafness Syndrome
|
|
Keratoderma Palmoplantar Deafness
|
Diffuse Palmoplantar Keratoderma With Deafness
|
|
Focal Palmoplantar Keratoderma With Sensorineural Deafness
|
Hereditary Palmoplantar Keratoderma With Deafness
|
|
Keratoderma Palmoplantar, With Deafness
|
Palmoplantar Keratoderma And Sensorineural Deafness
|
|
Ppk With Deafness
|
PPKDFN
|
|
Keratoderma Palmoplantar, Deafness
|
|
|
| Naxos Disease |
|
Mal De Naxos
|
NXD
|
|
Cardiomyopathy, Arrhythmogenic Right Ventricular, With Skin, Hair, And Nail Abnormalities
|
Woolly Hair, Palmoplantar Keratoderma, And Cardiac Abnormalities
|
|
Palmoplantar Keratoderma With Arrhythmogenic Right Ventricular Cardiomyopathy And Woolly Hair
|
Keratosis Palmoplantaris With Arrythmogenic Cardiomyopathy
|
|
Keratosis Palmoplantaris With Arrhythmogenic Cardiomyopathy
|
Keratosis Palmoplantaris Arrythmogenic Cardiomyopathy Woolly Hair
|
|
Woolly Hair Palmoplantar Keratoderma Cardiac Abnormalities
|
Kwwh Type I
|
|
Keratoderma With Woolly Hair Type I
|
Palmoplantar Hyperkeratosis With Arrythmogenic Cardiomyopathy
|
|
Palmoplantar Keratoderma With Arrythmogenic Cardiomyopathy
|
|
|
| Acute Chest Syndrome |
|
Acute Chest Syndrome In Sickle Cell Disease
|
|
|
| Vohwinkel Syndrome |
|
Mutilating Keratoderma
|
Keratoderma Hereditarium Mutilans
|
|
Khm
|
VOWNKL
|
|
Deafness, Congenital, With Keratopachydermia And Constrictions Of Fingers And Toes
|
Mutilating Keratoderma Of Vohwinkel
|
|
Mutilating Keratoderma Plus Deafness
|
Ppk Mutilans And Deafness
|
|
Congenital Deafness With Keratopachydermia And Constrictions Of Fingers And Toes
|
Congenital Deafness With Keratopachydermia And Constrictions Fo Fingers And Toes
|
|
Palmoplantar Keratoderma Mutilans
|
Palmoplantar Keratoderma Mutilans Vohwinkel
|
|
Ppk Mutilans Vohwinkel
|
Mutilating Keratoderma Plus Hearing Loss
|
|
Ppk Mutilans And Hearing Loss
|
|
|
| Leukodystrophy, Hypomyelinating, 2 |
|
Pmld1
|
Hypomyelinating Leukodystrophy 2
|
|
HLD2
|
Pelizaeus-Merzbacher-Like Disease 1
|
|
Pelizaeus-Merzbacher-Like Disease Due To Gjc2 Mutation
|
Pelizaeus-Merzbacher-Like Disease Type 1
|
|
Pelizaeus-Merzbacher-Like Disease, 1
|
Pelizaeus Merzbacher Like Disease
|
|
Pelizaeus-Merzbacher-Like Disease
|
Pmld - Pelizaeus Merzbacher Like Disease
|
|
Pelizaeus-Merzbacher-Like Disease Autosomal Recessive Type 1
|
Pmldar1
|
|
Leukodystrophy, Hypomyelinating, Type 2
|
|
|
| Ectodermal Dysplasia |
|
Congenital Ectodermal Defect
|
Congenital Ectodermal Dysplasia
|
|
Ectodermal Dysplasia Syndrome
|
Dysplasia, Ectodermal
|
|
|
| Brain Cancer |
|
Adult Brain Tumor
|
Malignant Neoplasm Of Brain
|
|
Brain Neoplasms
|
Brain Neoplasm
|
|
Neoplasm Of Brain
|
Primary Malignant Neoplasm Of Brain
|
|
Brain Tumors
|
Adult Malignant Brain Neoplasm
|
|
Brain Neoplasm, Adult
|
Bt - Brain Tumour
|
|
Malignant Brain Tumour
|
Malignant Primary Brain Neoplasm
|
|
Malignant Primary Brain Tumor
|
Malignant Tumor Of Adult Brain
|
|
Malignant Tumor Of Brain
|
Primary Brain Neoplasm
|
|
Primary Brain Tumor
|
Tumor Of The Brain
|
|
Brain Tumor, Adult
|
Brain Tumor Primary
|
|
Malignant Primary Brain Tumors
|
Primary Brain Tumors
|
|
Cancer, Brain
|
Brain Tumor, Primary
|
|
|
| Myocarditis |
|
Myocardial Inflammation
|
Inflammatory Cardiomyopathy
|
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| Cardiomyopathy, Dilated, With Woolly Hair And Keratoderma |
|
Carvajal Syndrome
|
Palmoplantar Keratoderma With Left Ventricular Cardiomyopathy And Woolly Hair
|
|
DCWHK
|
Dilated Cardiomyopathy With Woolly Hair And Keratoderma
|
|
Cardiomyopathy Dilated With Woolly Hair And Keratoderma
|
Kwwh Type Ii
|
|
Keratoderma With Woolly Hair Type Ii
|
Woolly Hair-Palmoplantar Hyperkeratosis-Dilated Cardiomyopathy Syndrome
|
|
Woolly Hair-Palmoplantar Keratoderma-Dilated Cardiomyopathy Syndrome
|
Wooly Hair-Palmoplantar Hyperkeratosis-Dilated Cardiomyopathy Syndrome
|
|
Wooly Hair-Palmoplantar Keratoderma-Dilated Cardiomyopathy Syndrome
|
Epidermolytic Palmoplantar Keratoderma Woolly Hair And Dilated Cardiomyopathy
|
|
Wooly Hair - Palmoplantar Keratoderma - Dilated Cardiomyopathy
|
Cardiomyopathy, Dilated With Woolly Hair And Keratoderma
|
|
|
| Dilated Cardiomyopathy |
|
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
|
Cardiomyopathy, Dilated
|
DCM
|
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|
| Syndromic X-Linked Intellectual Disability 34 |
|
Macrocephaly-Intellectual Disability-Left Ventricular Non Compaction Syndrome
|
Mental Retardation, X-Linked, Syndromic 34
|
|
Mrxs34
|
Mrxsml
|
|
Syndromic X-Linked Mental Retardation Mircsof-Langouet Type
|
|
|
| Palmoplantar Keratoderma, Nonepidermolytic |
|
Nonepidermolytic Palmoplantar Keratoderma
|
NEPPK
|
|
Tylosis
|
Unna-Thost Syndrome
|
|
Keratoderma, Palmoplantar, Diffuse
|
Ppkne
|
|
Keratoderma, Nonepidermolytic Palmoplantar
|
Diffuse Nonepidermolytic Palmomplantar Keratoderma
|
|
Thost-Unna Syndrome
|
Non-Epidermolytic Palmoplantar Keratoderma
|
|
Autosomal Dominant Diffuse Palmoplantar Keratoderma, Norrbotten Type
|
Diffuse Palmoplantar Keratoderma, Bothnian Type
|
|
Krt1-Related Diffuse Nonepidermolytic Keratoderma
|
Krt1-Related Diffuse Neppk
|
|
Keratoderma, Palmoplantar, Non-Epidermolytic
|
Nonepidermolytic Unna-Thost Disease
|
|
Non-Epidermolytic Unna-Thost Disease
|
Keratoderma, Palmoplantar, Nonepidermolytic
|
|
Hyperkeratosis
|
|
|
| Myocardial Infarction |
|
Heart Attack
|
Myocardial Infarction, Susceptibility To
|
|
Myocardial Infarction 1
|
Myocardial Infarction, Protection Against
|
|
Myocardial Infarction, Decreased Susceptibility To
|
Myocardial Infarction, Decreased
|
|
Myocardial Infarct
|
MCI1
|
|
Premature Myocardial Infarction
|
Myocardial Infarction, Susceptibility To, Type 1
|
|
|
| Cardiomyopathy, Dilated, 1o |
|
Dilated Cardiomyopathy 1o
|
CMD1O
|
|
Dilated Cardiomyopathy With Ventricular Tachycardia
|
Cardiomyopathy, Dilated, With Ventricular Tachycardia
|
|
Cardiomyopathy, Dilated 1o
|
Cardiomyopathy, Dilated, Type 1o
|
|
|
| Atrioventricular Block |
|
|
| Ichthyosis |
|
Ichthyoses
|
Non-Syndromic Ichthyosis
|
|
Congenital Ichthyosis
|
|
|
| Sudden Infant Death Syndrome |
|
SIDS
|
Sudden Infant Death Syndrome, Susceptibility To
|
|
Cot Death
|
Crib Death
|
|
Sudden Death Of Nonspecific Cause In Infancy
|
Sudden Infant Death
|
|
Death, Sudden, Syndrome, Infant
|
|
|
| Balo Concentric Sclerosis |
|
Balo'S Concentric Sclerosis
|
Balo Disease
|
|
Diffuse Cerebral Sclerosis Of Schilder
|
Tumefactive Multiple Sclerosis
|
|
Concentric Demyelination
|
Balo'S Disease
|
|
Baló Concentric Sclerosis
|
Encephalitis Periaxialis Concentrica
|
|
Marburg Variant
|
|
|
| Cataract |
|
Cataracts
|
Cat - [Cataract]
|
|
Cataract Form
|
Lens Opacity
|
|
Lens Opacities
|
|
|
| Lipoprotein Quantitative Trait Locus |
|
Coronary Artery Disease
|
Coronary Artery Anomaly
|
|
Coronary Artery Disease, Susceptibility To
|
Myocardial Ischemia
|
|
Congenital Anomaly Of Coronary Artery
|
Coronary Arteriosclerosis
|
|
Coronary Disease
|
Coronary Heart Disease
|
|
Coronary Artery Disorder
|
LPAQTL
|
|
Lpa Deficiency, Congenital
|
Coronary Artery Abnormality
|
|
Coronary Artery Anomaly, Congenital
|
Chd
|
|
Coronary Syndrome
|
Congenital Malformations Of Coronary Vessels
|
|
Malformation Of Coronary Vessels
|
Congenital Coronary Artery Anomaly
|
|
Congenital Coronary Artery Deformity
|
Congenital Coronary Artery Disorder
|
|
Abnormal Coronary Artery
|
Congenital Coronary Artery Malposition
|
|
Congenital Coronary Disease
|
Congenital Anomaly Of Coronary Arteries
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| 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
|
|
|
| Glioblastoma |
|
Glioblastoma Multiforme
|
Gbm
|
|
Adult Glioblastoma Multiforme
|
Grade Iv Adult Astrocytic Tumor
|
|
Primary Glioblastoma Multiforme
|
Spongioblastoma Multiforme
|
|
Adult Glioblastoma
|
Primary Glioblastoma
|
|
|
| Glioblastoma Classical Subtype |
|
|
| Megalencephalic Leukoencephalopathy With Subcortical Cysts |
|
Vacuolating Megalencephalic Leukoencephalopathy With Subcortical Cysts
|
Mlc
|
|
Van Der Knaap Disease
|
Lvm
|
|
Leukoencephalopathy With Swelling And Cysts
|
Megalencephaly-Cystic Leukodystrophy
|
|
Megalencephalic Leukodystrophy Megalencephaly-Cystic Leukodystorphy Syndrome
|
Infantile Leukoencephalopathy And Megalencephaly
|
|
Leukoencephalopathy With Swelling And A Discrepantly Mild Course
|
Vacuolating Leukoencephalopathy
|
|
Megalencephalic Leukodystrophy
|
Megalencephaly-Cystic Leukodystrophy Syndrome
|
|
Van Der Knaap Syndrome
|
Leukoencephalopathy, Megalencephalic, With Subcortical Cysts
|
|
|
| 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
|
|
|
| Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 |
|
CMTX1
|
Cmtx
|
|
Charcot-Marie-Tooth Disease X-Linked Dominant 1
|
Charcot-Marie-Tooth Neuropathy, X-Linked Dominant, 1
|
|
X-Linked Charcot-Marie-Tooth Disease
|
Charcot-Marie-Tooth Peroneal Muscular Atrophy, X-Linked
|
|
Cmt1x
|
X-Linked Charcot-Marie-Tooth Disease Type 1
|
|
X-Linked Hereditary Motor And Sensory Neuropathy
|
Hereditary Motor And Sensory Neuropathy, X-Linked
|
|
Hmsn, X-Linked
|
Charcot-Marie-Tooth Neuropathy, X-Linked, 1
|
|
Cmt2, Formerly
|
Charcot-Marie-Tooth Neuropathy X-Linked Dominant 1
|
|
Charcot-Marie-Tooth Neuropathy X-Linked 1
|
Charcot-Marie-Tooth Peroneal Muscular Atrophy X-Linked
|
|
Hereditary Motor And Sensory Neuropathy X-Linked
|
Hmsn X-Linked
|
|
Charcot-Marie-Tooth, X-Linked
|
Charcot-Marie-Tooth Disease, X-Linked Dominant, Type 1
|
|
Charcot-Marie-Tooth Disease, X-Linked, 1
|
|
|
| Intraocular Pressure Quantitative Trait Locus |
|
Glaucoma
|
IOPQTL
|
|
Glaucoma, Susceptibility To
|
Postinfectious Glaucoma
|
|
Glaucoma With Ocular Inflammation
|
Glaucoma Secondary To Eye Inflammation
|
|
Traumatic Glaucoma
|
Glaucoma With Concussion Of Globe
|
|
Glaucoma Due To Ocular Trauma
|
Glaucoma Associated With Ocular Trauma
|
|
Glaucoma Secondary To Drugs
|
|
|
| Familial Woolly Hair Syndrome |
|
Wooly Hair
|
Familial Wooly Hair Syndrome
|
|
Hereditary Woolly Hair Syndrome
|
Hereditary Wooly Hair Syndrome
|
|
Woolly Hair
|
Syndrome With Woolly Hair
|
|
Wooly Hair Syndrome
|
|
|
| Neurogenic Bladder |
|
Neurogenic Dysfunction Of The Urinary Bladder
|
Neurogenic Urinary Bladder Disorder
|
|
Neuropathic Bladder
|
Bladder Neurogenic
|
|
Urinary Bladder, Neurogenic
|
Neurogenic Urinary Bladder
|
|
|
| Intrinsic Cardiomyopathy |
|
|
| Muscular Dystrophy |
|
Muscular Dystrophies
|
Congenital Md
|
|
Congenital Muscular Dystrophy
|
Cmd
|
|
Mdc
|
Dystrophy, Muscular
|
|
Gower'S Muscular Dystrophy
|
Progressive Musclular Dystrophy
|
|
Pseudohypertrophic Atrophy
|
Pseudohypertrophic Muscle Paralysis
|
|
Pseudohypertrophic Muscular Atrophy
|
Pseudohypertrophic Muscular Dystrophy
|
|
Pseudohypertrophic Paralysis
|
Pseudomuscular Hypertrophy
|
|
|
| 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
|
|
|
| Epilepsy |
|
Epilepsy Syndrome
|
Epileptic Syndrome
|
|
Epilepsies
|
Symptomatic Epilepsies
|
|
Post Traumatic Epilepsy
|
Traumatic Epilepsy
|
|
Traumatic Epileptic
|
Epilepsy Due To Hippocampal Sclerosis
|
|
Epilepsy With Ammon'S Horn Sclerosis
|
Epilepsy Due To Cortical Dysplasia
|
|
Epilepsy Due To Neuronal Migration Disorders
|
|
|
| High Grade Glioma |
|
Malignant Glioma
|
Glial Cell Tumor
|
|
Glioma, Malignant
|
Malignant Neuroglial Tumor
|
|
Neuroglial Tumor
|
Glioma
|
|
Malignant Gliomas
|
|
|
| Fanconi Renotubular Syndrome 1 |
|
Renal Fanconi Syndrome
|
Adult Fanconi Syndrome
|
|
FRTS1
|
Fanconi Renotubular Syndrome
|
|
Frts
|
Rfs
|
|
Fanconi Syndrome Without Cystinosis
|
Luder-Sheldon Syndrome
|
|
|
| Gliosarcoma |
|
Glioblastoma With Sarcomatous Component
|
Sarcomatous Glioblastoma
|
|
|
| Heart Septal Defect |
|
Septal Defect
|
Heart Septal Defects
|
|
Cardiac Septal Defects
|
Congenital Septal Defect Of Heart
|
|
|
| Catecholaminergic Polymorphic Ventricular Tachycardia |
|
Cpvt
|
Catecholamine-Induced Polymorphic Ventricular Tachycardia
|
|
Familial Polymorphic Ventricular Tachycardia
|
Malignant Paroxysmal Ventricular Tachycardia
|
|
Multifocal Ventricular Premature Beats
|
Stress-Induced Polymorphic Ventricular Tachycardia
|
|
Bidirectional Tachycardia Induced By Catecholamine
|
Double Tachycardia Induced By Catecholamines
|
|
Polymorphic Catecholergic Ventricular Tachycardia
|
Syncopal Paroxysmal Tachycardia
|
|
Bidirectional Tachycardia Induced By Catecholamines
|
Fpvt
|
|
Bidirectional Ventricular Tachycardia Induced By Catecholamine
|
Polymorphic Ventricular Tachycardia Induced By Catecholamines
|
|
Ventricular Tachycardia, Catecholaminergic Polymorphic
|
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1
|
|
Familial Ventricular Tachycardia
|
Multifocal Pvcs
|
|
Multifocal Premature Ventricular Beats
|
|
|
| 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
|
|
|
| Double Outlet Right Ventricle |
|
Double Outlet Right Ventricle With Subpulmonary Ventricular Septal Defect
|
Taussig-Bing Syndrome
|
|
Dextrotransposition Of Aorta
|
Taussig-Bing Syndrome Or Defect
|
|
Dorv
|
Dorv With Subpulmonary Vsd
|
|
Dorv-Tga
|
Double Outlet Right Ventricle With Transposition Of The Great Arteries
|
|
Double Outlet Right Ventricle With Subpulmonary Interventricular Communication, Transposition Type
|
Taussig-Bing Heart
|
|
Taussig-Bing Malformation
|
Taussig-Bing Complex
|
|
Taussig-Bing Defect
|
Taussig-Bing
|
|
Double Outlet Right Ventricle With Remote Ventricular Septal Defect
|
Double Outlet Right Ventricle With Uncommitted Ventricular Septal Defect
|
|
Double Outlet Right Ventricle With Non-Committed Interventricular Communication
|
Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication Without Pulmonary Stenosis
|
|
Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication And Pulmonary Stenosis
|
|
|
| Type 1 Diabetes Mellitus 12 |
|
Diabetes Mellitus, Insulin-Dependent, 12
|
IDDM12
|
|
Insulin-Dependent Diabetes Mellitus 12
|
T1D12
|
|
Type 1 Diabetes Mellitus 12, Susceptibility To
|
Diabetes Mellitus, Insulin-Dependent, Type 12
|
|
|
| Brugada Syndrome |
|
Sudden Unexpected Nocturnal Death Syndrome
|
Sudden Unexplained Nocturnal Death Syndrome
|
|
Bangungut
|
Brugada Type Idiopathic Ventricular Fibrillation
|
|
Pokkuri Death Syndrome
|
Sunds
|
|
Idiopathic Ventricular Fibrillation, Brugada Type
|
Sudden Unexplained Death
|
|
Dream Disease
|
Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome
|
|
Sudden Unexplained Death Syndrome
|
Suds
|
|
Sunds - [Sudden Unexplained Nocturnal Death Syndrome]
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Spermatogenic Failure |
|
Azoospermia
|
Spgf
|
|
Spermatogenic Failure, Susceptibility To
|
Absent Sperm
|
|
Aspermatogenesis
|
Infertility Due To Azoospermia
|
|
Hypospermatogenesis
|
Azoospermatism
|
|
|
| Ventricular Septal Defect |
|
Ventricular Septal Defects
|
Interventricular Septal Defect
|
|
Heart Septal Defects, Ventricular
|
Ventricular Septal Abnormality
|
|
Interventricular Septum Defect
|
Ventricular Septum Defect
|
|
Vsd - [Ventricular Septum Defect]
|
Congenital Ventricular Septal Defect
|
|
Single Ventricular Septal Defect
|
|
|
| Stroke, Ischemic |
|
Cerebral Infarction
|
Stroke
|
|
Ischemic Stroke
|
Cerebrovascular Accident
|
|
Cerebral Infarction, Susceptibility To
|
Stroke, Ischemic, Susceptibility To
|
|
Cerebral Infarct
|
Ischemic Stroke, Susceptibility To
|
|
Stroke, Susceptibility To
|
Cva - Cerebral Infarction
|
|
ISCHSTR
|
Ischemic Cerebrovascular Accident
|
|
|
| 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
|
|
|
| Hypertension, Essential |
|
Essential Hypertension
|
Hypertension
|
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
|
Hypertensive Disease
|
Primary Hypertension
|
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
|
Hyperpiesia
|
Idiopathic Hypertension
|
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
|
Htn
|
Vascular Hypertensive Disorder
|
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
|
Arterial Hypertension Nos
|
Hypertension Nos
|
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
|
Systemic Hypertension
|
Artery Htn
|
|
Benign Htn
|
Vascular Htn
|
|
Vascular Hypertension
|
Cholesterol Hypertension
|
|
Cholesterol Htn
|
Idiopathic Htn
|
|
Malignant Hypertension
|
Malignant Htn
|
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
|
Hypertensive Vascular Degeneration
|
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt Syndrome
|
|
|
| Atrial Heart Septal Defect |
|
Atrial Septal Defect
|
Atrial Septal Defects
|
|
Atrioseptal Defect
|
Auricular Septal Defect
|
|
Congenital Atrial Septal Defect
|
Interatrial Septal Defect
|
|
Interauricular Septal Defect
|
Heart Septal Defects, Atrial
|
|
Septal Defect, Atrial
|
|
|
| Hypomyelinating Leukodystrophy |
|
Hld
|
Leukodystrophy, Hypomyelinating
|
|
|
| Familial Atrial Fibrillation |
|
Atrial Fibrillation, Familial
|
Atfb
|
|
Atrial Fibrillation Autosomal Dominant
|
Autosomal Dominant Atrial Fibrillation
|
|
Auricular Fibrillation
|
Atrial Fibrillation
|
|
Atrial Fibrillation, Familial, 1
|
|
|
| Left Ventricular Noncompaction |
|
Noncompaction Cardiomyopathy
|
Left Ventricular Hypertrabeculation
|
|
Lvnc
|
Spongy Myocardium
|
|
Isolated Noncompaction Of The Ventricular Myocardium
|
Left Ventricular Myocardial Noncompaction Cardiomyopathy
|
|
Fetal Myocardium
|
Honeycomb Myocardium
|
|
Hypertrabeculation Syndrome
|
Left Ventricular Non-Compaction
|
|
Lvht
|
Non-Compaction Of The Left Ventricular Myocardium
|
|
Ventricular Noncompaction, Left
|
Non-Compaction Cardiomyopathy
|
|
|
| Hypertrophic Cardiomyopathy |
|
Hypertrophic Obstructive Cardiomyopathy
|
Cardiomyopathy, Hypertrophic
|
|
Cardiomyopathy Hypertrophic Obstructive
|
Cardiomyopathy, Hypertrophic, Familial
|
|
Idiopathic Myocardial Hypertrophy
|
Idiopathic Hypertrophic Cardiomyopathy
|
|
Obstructive Idiopathic Hypertrophic Cardiomyopathy
|
Obstructive Cardiomyopathy
|
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Muscular Subaortic Stenosis
|
|
Hypertrophic Obstructive Subaortic Stenosis
|
|
|
| Alzheimer Disease, Familial, 1 |
|
Alzheimer Disease
|
Alzheimer'S Disease
|
|
Presenile And Senile Dementia
|
AD1
|
|
Alzheimer Disease, Susceptibility To
|
Alzheimer Disease, Late-Onset, Susceptibility To
|
|
Alzheimer Disease 1, Familial
|
AD
|
|
Familial Alzheimer Disease
|
Alzheimer Disease, Late-Onset
|
|
Alzheimers Dementia
|
Alzheimer Dementia
|
|
Alzheimer Sclerosis
|
Alzheimer Syndrome
|
|
Alzheimer-Type Dementia
|
Dat
|
|
Primary Senile Degenerative Dementia
|
Sdat
|
|
Alzheimer Disease 1
|
Autosomal Dominant Alzheimer Disease
|
|
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
|
Late Onset Alzheimer Disease
|
|
Alzheimers Disease
|
Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
|
|
Late-Onset Alzheimers Disease
|
Alzheimer'S Disease Pathway Kegg
|
|
Dementia Due To Alzheimer'S Disease
|
Alzheimer Disease Type 1
|
|
Alzheimers
|
|
|
| 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
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Amyotrophic Lateral Sclerosis 1 |
|
Amyotrophic Lateral Sclerosis
|
ALS
|
|
Lou Gehrig Disease
|
Amyotrophic Lateral Sclerosis Type 1
|
|
Charcot Disease
|
ALS1
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To
|
Fals
|
|
Lou Gehrig'S Disease
|
Mnd
|
|
Motor Neuron Disease
|
Familial Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis 1, Familial
|
Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
|
Motor Neuron Disease, Bulbar
|
Motor Neurone Disease
|
|
Amyotrophic Lateral Sclerosis With Dementia
|
Dementia With Amyotrophic Lateral Sclerosis
|
|
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
|
Sclerosis, Lateral, Amyotrophic
|
|
Sclerosis, Lateral, Amyotrophic, Type 1
|
Amyotrophic Sclerosis
|
|
Als - [Amyotrophic Lateral Sclerosis]
|
Wasting Palsy
|
|
Amyotrophic Paralysis
|
Amyotrophy Lateral Sclerosis
|
|
Wasting Paralysis
|
Spinal Progressive Amyotrophy
|
|
Progressive Atrophic Paralysis
|
|
|
