| Diseases |
Alias |
|
| Wolfram-Like Syndrome, Autosomal Dominant |
|
Wolfram-Like Syndrome
|
WFSL
|
|
Hearing Loss, Progressive, With Optic Atrophy And/Or Impaired Glucose Regulation
|
Wolfram-Like Syndrome Autosomal Dominant
|
|
Hearing Loss Progressive With Optic Atrophy And/Or Impaired Glucose Regulation
|
Wolfram Syndrome-Like Disease
|
|
Wolfram-Like Disorder
|
|
|
| Cataract 41 |
|
CTRCT41
|
Cataract 41, Congenital Nuclear Type
|
|
Congenital Nuclear Type Cataract 41
|
Congenital Nuclear Cataract 41
|
|
Cataract, Type 41
|
|
|
| Wolfram Syndrome 1 |
|
WFS1
|
Didmoad
|
|
Wfs
|
Diabetes Mellitus And Insipidus With Optic Atrophy And Deafness
|
|
Diabetes Insipidus And Mellitus With Optic Atrophy And Deafness
|
Diabetes Insipidus And Mellitus With Optic Atrophy And Deafness Syndrome
|
|
Wolfram Syndrome
|
|
|
| Deafness, Autosomal Dominant 6 |
|
DFNA6
|
Dfna14
|
|
Dfna38
|
Deafness, Autosomal Dominant 6/14/38
|
|
Autosomal Dominant Nonsyndromic Deafness 6
|
Deafness, Autosomal Dominant 14
|
|
Deafness, Autosomal Dominant 38
|
Autosomal Dominant Deafness 14
|
|
Autosomal Dominant Deafness 38
|
Autosomal Dominant Deafness 6
|
|
Deafness, Autosomal Dominant, 6
|
Deafness Autosomal Dominant 14
|
|
Deafness Autosomal Dominant 38
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 6
|
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 6
|
|
|
| Wolfram Syndrome |
|
Didmoad Syndrome
|
Didmoad
|
|
Diabetes Insipidus And Mellitus With Optic Atrophy And Deafness
|
Wfs
|
|
Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, And Deafness
|
Didmoadud
|
|
Diabetes Insipidus-Diabetes Mellitus-Optic Atrophy-Deafness Syndrome
|
Diabetes Insipidus-Diabetes Mellitus-Optic Atrophy-Hearing Loss Syndrome
|
|
|
| Hydronephrosis |
|
Stricture Of Ureteropelvic Junction With Hydronephrosis
|
Hydronephrosis With Ureteral Stricture, Not Elsewhere Classified
|
|
|
| Diaphragm Disease |
|
Abnormality Of The Diaphragm
|
Disease Of Diaphragm
|
|
Diaphragmatic Disorder
|
Disorder Of Diaphragm
|
|
|
| Duane Retraction Syndrome 1 |
|
Duane Syndrome
|
Duane Retraction Syndrome
|
|
Drs
|
Duane Anomaly
|
|
Stilling-Turk-Duane Syndrome
|
DURS1
|
|
Dus
|
Retraction Syndrome
|
|
Duane Anomaly, Isolated
|
Type 1 Duane Retraction Syndrome
|
|
|
| Laryngomalacia |
|
Congenital Laryngomalacia
|
Congenital Laryngeal Stridor
|
|
Laryngomalacia Congenital
|
Floppy Epiglottis
|
|
|
| Diabetes Mellitus |
|
|
| Diaphragmatic Eventration |
|
|
| Duane Retraction Syndrome |
|
Stilling-Turk-Duane Syndrome
|
Duane'S Syndrome
|
|
Duane Syndrome
|
Isolated Duane Retraction Syndrome
|
|
Co-Contractive Retraction Syndrome
|
Duane Anomaly, Isolated
|
|
Ocular Retraction Syndrome
|
Drs
|
|
Durs
|
|
|
| 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
|
|
|
| Night Blindness |
|
|
| 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
|
|
|
| Dandy-Walker Syndrome |
|
Dandy-Walker Malformation
|
DWS
|
|
Atresia Of Foramina Of Magendie And Luschka
|
Dandy-Walker Complex
|
|
Dandy-Walker Cyst
|
Dandy-Walker Deformity
|
|
Dandy Walker Cyst
|
Dw Complex
|
|
Dandy-Walker Syndrome Or Malformation
|
Dandy-Walker Variant
|
|
Mega Cisterna Magna
|
Dwm
|
|
Hydrocephalus, Internal, Dandy-Walker Type
|
Hydrocephalus, Noncommunicating, Dandy-Walker Type
|
|
Luschka-Magendie Foramina Atresia
|
Isolated Dandy-Walker Malformation
|
|
Mega-Cisterna Magna
|
Dandy Walker Variant
|
|
Atresia Of Foramen Of Luschka
|
Atresia Of Foramen Of Magendie
|
|
Congenital Blockage Of Foramen Magendie
|
|
|
| Cleft Palate, Isolated |
|
Cleft Palate
|
Isolated Cleft Palate
|
|
CPI
|
Cp
|
|
Palatoschisis
|
Cleft Palate Isolated
|
|
Uranostaphyloschisis
|
Congenital Fissure Of Palate
|
|
Cleft Of Secondary Palate
|
|
|
| Early-Onset Nuclear Cataract |
|
|
| Rare Genetic Deafness |
|
Rare Genetic Hearing Loss
|
|
|
| Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna |
|
Autosomal Dominant Isolated Neurosensory Deafness Type Dfna
|
Autosomal Dominant Isolated Neurosensory Hearing Loss Type Dfna
|
|
Autosomal Dominant Isolated Sensorineural Deafness Type Dfna
|
Autosomal Dominant Isolated Sensorineural Hearing Loss Type Dfna
|
|
Autosomal Dominant Non-Syndromic Neurosensory Deafness Type Dfna
|
Autosomal Dominant Non-Syndromic Neurosensory Hearing Loss Type Dfna
|
|
Autosomal Dominant Non-Syndromic Sensorineural Hearing Loss Type Dfna
|
|
|
| Diabetes Insipidus |
|
|
| Wolfram Syndrome 2 |
|
|
| Insulinoma |
|
Islet Cell Adenoma
|
Insulin-Producing Tumor Of Islet Cells
|
|
Adenoma Islet Cell
|
Islet Cell Tumor
|
|
Experimental Organism Islet Cell Adenoma Neoplasm
|
|
|
| 3-Methylglutaconic Aciduria, Type Iii |
|
Optic Atrophy
|
3-Methylglutaconic Aciduria Type 3
|
|
Costeff Syndrome
|
Mga3
|
|
Costeff Optic Atrophy Syndrome
|
Optic Atrophy Plus Syndrome
|
|
Infantile Optic Atrophy With Chorea And Spastic Paraplegia
|
3-Methylglutaconic Aciduria Type Iii
|
|
Autosomal Recessive Optic Atrophy Plus Syndrome
|
Autosomal Recessive Optic Atrophy Type 3
|
|
Opa3 Defect
|
MGCA3
|
|
Mga, Type Iii
|
Iraqi Jewish Optic Atrophy Plus
|
|
Mga Type Iii
|
Optic Atrophy, Infantile, With Chorea And Spastic Paraplegia
|
|
Iraqi-Jewish 'Optic Atrophy Plus'
|
Optic Atrophy 3, Autosomal Recessive
|
|
Opa3, Autosomal Recessive
|
Opa3-Related 3-Methylglutaconic Aciduria
|
|
Iraqi-Jewish Optic Atrophy Plus
|
Atrophy Of Optic Disc
|
|
3-Alpha Methylglutaconic Aciduria Type Iii
|
Optic Atrophy 3
|
|
Optic Atrophy Infantile With Chorea And Spastic Paraplegia
|
Autosomal Recessive Opa3
|
|
Autosomal Recessive Optic Atrophy 3
|
3-Methylglutaconic Aciduria 3
|
|
3-Alpha-Methylglutaconic Aciduria Type 3
|
Optic Atrophy 3 Autosomal Recessive
|
|
Atrophy, Optic
|
Atrophy, Optic, Plus Syndrome
|
|
Optic Nerve Atrophy
|
Primary Optic Atrophy
|
|
Oa - [Optic Atrophy]
|
Second Cranial Nerve Atrophy
|
|
Second Cranium Nerve Atrophy
|
|
|
| Nonsyndromic Hearing Loss |
|
Nonsyndromic Deafness
|
Nonsyndromic Hearing Impairment
|
|
Nonsyndromic Hearing Loss And Deafness
|
Deafness, Nonsyndromic
|
|
Isolated Deafness
|
|
|
| Spastic Ataxia |
|
|
| Deafness, Autosomal Dominant 1, With Or Without Thrombocytopenia |
|
Konigsmark Syndrome
|
DFNA1
|
|
Autosomal Dominant Nonsyndromic Deafness 1
|
Lfhl1
|
|
Deafness, Autosomal Dominant 1
|
Autosomal Dominant Deafness 1
|
|
Autosomal Dominant Deafness 1, With Or Without Thrombocytopenia
|
Hereditary Low Frequency Hearing Loss 1
|
|
Diaph1-Related Sensorineural Hearing Loss-Thrombocytopenia Syndrome
|
Diaph1-Related Sensorineural Deafness-Thrombocytopenia Syndrome
|
|
Hereditary Low-Frequency Hearing Loss
|
Hereditary Low-Frequency Sensorineural Hearing Loss
|
|
Lfsnhl1
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 1
|
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 1
|
Deafness, Autosomal Dominant, Type 1
|
|
|
| Thiamine-Responsive Megaloblastic Anemia Syndrome |
|
TRMA
|
Rogers Syndrome
|
|
Thiamine-Responsive Myelodysplasia
|
Thiamine-Responsive Anemia Syndrome
|
|
Thiamine Metabolism Dysfunction Syndrome 1
|
Thmd1
|
|
Megaloblastic Anemia, Thiamine-Responsive, With Diabetes Mellitus And Sensorineural Deafness
|
Thiamine-Responsive Megaloblastic Anemia With Diabetes Mellitus And Sensorineural Deafness
|
|
Thiamine Responsive Megaloblastic Anemia Syndrome
|
Megaloblastic Anemia Thiamine-Responsive With Diabetes Mellitus And Sensorineural Deafness
|
|
Thiamine-Responsive Megaloblastic Anemia
|
Thiamine-Responsive Anaemia Syndrome
|
|
Thiamine-Responsive Megaloblastic Anaemia Syndrome
|
Thiamine-Responsive Megaloblastic Anaemia With Diabetes Mellitus And Sensorineural Deafness
|
|
Thiamine-Responsive Megaloblastic Anemia With Diabetes Mellitus And Sensorineural Hearing Loss
|
|
|
| Cranial Nerve Disease |
|
Cranial Nerve Disorder
|
Disorder Of Cranial Nerve
|
|
Cranial Nerve Diseases
|
|
|
| Optic Atrophy With Or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, And Neuropathy |
|
Dominant Optic Atrophy Plus Syndrome
|
DOA+
|
|
Adoa
|
Autosomal Dominant Optic Atrophy
|
|
Doa
|
Optic Atrophy Plus Syndrome
|
|
Dominant Optic Atrophy
|
Optic Atrophy With Or Without Deafness Ophthalmoplegia Myopathy Ataxia And Neuropathy
|
|
Optic Atrophy, Dominant
|
3-Methylglutaconic Aciduria Type 3
|
|
Optic Atrophy, Autosomal Dominant
|
|
|
| Optic Atrophy 7 With Or Without Auditory Neuropathy |
|
Optic Atrophy 7
|
OPA7
|
|
Autosomal Recessive Optic Atrophy, Opa7 Type
|
Optic Atrophy-7
|
|
Atrophy, Optic, Type 7, With/Without Auditory Neuropathy
|
|
|
| Cataract |
|
Cataracts
|
Cat - [Cataract]
|
|
Cataract Form
|
Lens Opacity
|
|
Lens Opacities
|
|
|
| Neuropathy |
|
Peripheral Neuropathy
|
Peripheral Neuropathies
|
|
|
| Epiphyseal Dysplasia, Multiple, With Early-Onset Diabetes Mellitus |
|
Wolcott-Rallison Syndrome
|
Med-Iddm Syndrome
|
|
Iddm-Med Syndrome
|
Wolcott Rallison Syndrome
|
|
WRS
|
Epiphyseal Dysplasia Multiple With Early-Onset Diabetes Mellitus
|
|
Early-Onset Diabetes Mellitus With Multiple Epiphyseal Dysplasia
|
Multiple Epiphyseal Dysplasia With Early-Onset Diabetes Mellitus
|
|
|
| Optic Atrophy 6 |
|
OPA6
|
Optic Atrophy, Congenital Or Early Infantile, Autosomal Recessive
|
|
|
| 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
|
|
|
| Bipolar Disorder |
|
Bipolar Depression
|
Manic Disorder
|
|
Depression, Bipolar
|
Bipolar Disorder Manic Phase
|
|
Depressive-Manic Psych.
|
Manic Bipolar Affective Disorder
|
|
Manic Bipolar I Disorder
|
Manic Depression
|
|
Manic Depressive Disorder
|
Mixed Bipolar Disorder
|
|
Bipolar Affective Disorder
|
Bipolar Affective Psychosis
|
|
Bipolar Spectrum Disorder
|
Manic Depressive Illness
|
|
Depression Bipolar
|
Bipolar Disorder, Mixed
|
|
Major Affective Disorder
|
Major Affective Disorder 1
|
|
Major Affective Disorder 2
|
|
|
| Deafness, Autosomal Recessive 18a |
|
Deafness, Autosomal Recessive 18
|
DFNB18A
|
|
Dfnb18
|
Autosomal Recessive Nonsyndromic Deafness 18a
|
|
Autosomal Recessive Deafness 18a
|
Deafness, Autosomal Recessive, 18a
|
|
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 18
|
Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 18
|
|
Deafness, Autosomal Recessive, Type 18a
|
|
|
| Deafness, Autosomal Dominant 13 |
|
DFNA13
|
Autosomal Dominant Nonsyndromic Deafness 13
|
|
Autosomal Dominant Deafness 13
|
Deafness, Autosomal Dominant, 13
|
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 13
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 13
|
|
Deafness, Autosomal Dominant, Type 13
|
|
|
| Wolf-Hirschhorn Syndrome |
|
Pitt-Rogers-Danks Syndrome
|
WHS
|
|
Chromosome 4p16.3 Deletion Syndrome
|
Wittwer Syndrome
|
|
4p- Syndrome
|
Pitt Syndrome
|
|
4p Deletion Syndrome
|
Distal Deletion 4p
|
|
Distal Monosomy 4p
|
Telomeric Deletion 4p
|
|
Prds
|
4p Syndrome
|
|
Chromosome 4p Syndrome
|
Microcephaly, Iugr, Hypertelorism, Ptosis, Iris Coloboma, Hooked Nose, External Ear Dysplasia, Psychomotor Retardation
|
|
Wolf Syndrome
|
Chromosome 4p Deletion Syndrome
|
|
Chromosome 4p Monosomy
|
Del Syndrome
|
|
Monosomy 4p
|
Partial Monosomy 4p
|
|
Chromosome 4 Short Arm Deletion
|
|
|
| Dipsogenic Diabetes Insipidus |
|
Primary Polydipsia
|
Doid:0081058
|
|
Psychogenic Polydipsia
|
|
|
| Deafness, Autosomal Dominant 9 |
|
DFNA9
|
Autosomal Dominant Nonsyndromic Deafness 9
|
|
Autosomal Dominant Deafness 9
|
Deafness, Autosomal Dominant, 9
|
|
Deafness, Autosomal Dominant, Type 9
|
|
|
| Optic Nerve Disease |
|
Optic Neuropathy
|
Disorder Of The Second Nerve
|
|
Optic Nerve Disorder
|
Optic Nerve
|
|
Abnormality Of The Optic Nerve
|
Optic Nerve Disorders
|
|
Neuropathy, Optic
|
Disorder Of The Optic Nerve
|
|
|
| Asperger Syndrome |
|
Asperger Disorder
|
Asperger Syndrome, Susceptibility To
|
|
|
| Deafness, Autosomal Dominant 44 |
|
DFNA44
|
Autosomal Dominant Nonsyndromic Deafness 44
|
|
Autosomal Dominant Deafness 44
|
Deafness, Autosomal Dominant, 44
|
|
Deafness, Autosomal Dominant, Type 44
|
|
|
| Infantile Cerebellar-Retinal Degeneration |
|
ICRD
|
Infantile Cerebellar Retinal Degeneration
|
|
Degeneration, Cerebellar-Retinal, Infantile
|
|
|
| Gestational Diabetes Insipidus |
|
Transient Diabetes Insipidus Of Pregnancy
|
Diabetes Insipidus Gestational
|
|
Gestagenic Diabetes Insipidus
|
Doid:0081057
|
|
|
| Neonatal Diabetes |
|
Neonatal Diabetes Mellitus
|
Diabetes Mellitus Syndrome In Newborn Infant
|
|
Ndm
|
|
|
| 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
|
|
|
| Auditory System Disease |
|
Ear Diseases
|
Ear And Mastoid Disease
|
|
|
| Pontocerebellar Hypoplasia, Type 1e |
|
Pontocerebellar Hypoplasia Type 1
|
PCH1E
|
|
Norman Disease
|
Pch1
|
|
Pontocerebellar Hypoplasia With Anterior Horn Cell Disease
|
Pontocerebellar Hypoplasia With Infantile Spinal Muscular Atrophy
|
|
Pontocerebellar Hypoplasia Type 1e
|
Pontocerebellar Hypoplasia 1e
|
|
Doid:0112322
|
Doid:0112330
|
|
|
| Mood Disorder |
|
Mood Disorders
|
Episodic Mood Disorder
|
|
|
| Cortical Deafness |
|
|
| Permanent Neonatal Diabetes Mellitus |
|
Pndm
|
Permanent Diabetes Mellitus Of Infancy
|
|
Pdmi
|
Neonatal Diabetes Mellitus, Permanent
|
|
|
| Maturity-Onset Diabetes Of The Young, Type 2 |
|
Maturity-Onset Diabetes Of The Young Type 2
|
MODY2
|
|
Mody Glucokinase-Related
|
Mody Type 2
|
|
Mody, Type 2
|
Mody, Glucokinase-Related
|
|
Mody, Type Ii
|
Maturity-Onset Diabetes Of The Young 2
|
|
Mody-2
|
Diabetes Of The Young, Maturity-Onset, Type 2
|
|
Diabetes Mellitus Autosomal Dominant Type Ii
|
|
|
| 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
|
|
|
| Neurogenic Bladder |
|
Neurogenic Dysfunction Of The Urinary Bladder
|
Neurogenic Urinary Bladder Disorder
|
|
Neuropathic Bladder
|
Bladder Neurogenic
|
|
Urinary Bladder, Neurogenic
|
Neurogenic Urinary Bladder
|
|
|
| Inner Ear Disease |
|
Labyrinthine Dysfunction
|
Diseases Of Inner Ear
|
|
Labyrinthine Disease
|
Abnormality Of The Inner Ear
|
|
Labyrinth Diseases
|
Labyrinthine Disorder
|
|
Nonfunctioning Labyrinth
|
Labyrinthine Loss Of Function
|
|
Labyrinthine Syndrome
|
Labyrinthine Disorder Nos
|
|
|
| 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
|
|
|
| Deafness, Autosomal Dominant 4a |
|
Deafness, Autosomal Dominant 4
|
DFNA4A
|
|
Dfna4
|
Autosomal Dominant Nonsyndromic Deafness 4a
|
|
Autosomal Dominant Deafness 4a
|
Deafness, Autosomal Dominant, 4a
|
|
Deafness Autosomal Dominant 4
|
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 4
|
|
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 4
|
Deafness, Autosomal Dominant, Type 4a
|
|
|
| Maturity-Onset Diabetes Of The Young, Type 3 |
|
Maturity-Onset Diabetes Of The Young Type 3
|
MODY3
|
|
Mody, Type Iii
|
Mody Type 3
|
|
Mody, Type 3
|
Maturity-Onset Diabetes Of The Young 3
|
|
Mody-3
|
Diabetes Of The Young, Maturity-Onset, Type 3
|
|
|
| Maturity-Onset Diabetes Of The Young, Type 1 |
|
Maturity-Onset Diabetes Of The Young Type 1
|
MODY1
|
|
Mild Juvenile Diabetes Mellitus
|
Mody, Type I
|
|
Diabetes Mellitus Type 2
|
Mody Type 1
|
|
Mody, Type 1
|
Maturity-Onset Diabetes Of The Young 1
|
|
Mody-1
|
Diabetes Of The Young, Maturity-Onset, Type 1
|
|
|
| Cornelia De Lange Syndrome 1 |
|
De Lange Syndrome
|
CDLS1
|
|
Cdl
|
Cdls
|
|
Typus Degenerativus Amstelodamensis
|
Brachmann-De Lange Syndrome
|
|
Bdls
|
Amstelodamensis Typus Degenerativus
|
|
Cornelia De Lange Syndrome, Type 1
|
|
|
| Autosomal Dominant Nonsyndromic Deafness |
|
Autosomal Dominant Deafness
|
|
|
| Leber Hereditary Optic Neuropathy, Modifier Of |
|
Leber Optic Atrophy
|
Leber Hereditary Optic Neuropathy
|
|
LHON
|
Leber'S Hereditary Optic Neuropathy
|
|
Leber Optic Atrophy, Susceptibility To
|
Leber'S Optic Atrophy
|
|
LOAM
|
Loas
|
|
Leber'S Disease
|
Leber'S Optic Neuropathy
|
|
Optic Atrophy, Hereditary, Leber
|
Lhon, Modifier Of
|
|
Optic Atrophy, Leber Type
|
Hereditary Optic Neuroretinopathy
|
|
Leber Hereditary Optic Atrophy
|
Loa
|
|
Optic Atrophy Leber Type
|
Leber Hereditary Optic Neuropathy, Modifier
|
|
Leber Hereditary Optic Neuropathy Susceptibility
|
Modifier Of Leber Hereditary Optic Neuropathy
|
|
Lebers Hereditary Optic Neuropathy
|
Leber Congenital Amaurosis
|
|
|
| Leber Plus Disease |
|
Leber Congenital Amaurosis
|
Lca
|
|
Leber'S Amaurosis
|
Leber'S Disease
|
|
Amaurosis Congenita Of Leber
|
Amaurosis Congenita Of Leber, Type 1
|
|
Lhon Plus Disease
|
Congenital Absence Of The Rods And Cones
|
|
Congenital Retinal Blindness
|
Crb
|
|
Congenital Amaurosis Of Retinal Origin
|
Leber'S Congenital Amaurosis
|
|
Leber Congenital Amaurosis 1
|
Leber'S Congenital Tapetoretinal Degeneration
|
|
Leber'S Congenital Tapetoretinal Dysplasia
|
Lca1
|
|
Leber Congenital Amaurosis Type 1
|
Retinal Blindness, Congenital
|
|
Amaurosis, Leber Congenital
|
Dysgenesis Neuroepithelialis Retinae
|
|
Hereditary Epithelial Dysplasia Of Retina
|
Hereditary Retinal Aplasia
|
|
Heredoretinopathia Congenitalis
|
Leber Abiotrophy
|
|
Leber Congenital Tapetoretinal Degeneration
|
Lebers Congenital Amaurosis
|
|
Optic Atrophy, Hereditary, Leber
|
|
|
| Usher Syndrome |
|
Deafness-Retinitis Pigmentosa Syndrome
|
Dystrophia Retinae Pigmentosa-Dysostosis Syndrome
|
|
Graefe-Usher Syndrome
|
Hallgren Syndrome
|
|
Usher'S Syndrome
|
Retinitis Pigmentosa-Deafness Syndrome
|
|
Retinitis Pigmentosa-Hearing Loss Syndrome
|
Ush
|
|
Usher Syndromes
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| 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
|
|
|
