Disease Browser
Parent Node: Hearing Loss (D034381) ..Starting node .. Deafness (D003638) Child Nodes:
........Albinism deafness syndrome (C537042) ........ALPORT SYNDROME, X-LINKED (OMIM:301050) ........Arthrogryposis multiplex with deafness, inguinal hernias, and early death (C535381) ........Ayazi syndrome (C537793) ........Branchiogenic-Deafness Syndrome (C563780) ........Burn-Mckeown syndrome (C537411) ........Cardioauditory syndrome of Sanchez Cascos (C535577) ........Charcot-Marie-Tooth Disease, Demyelinating, Type 1e (C566136) ........Corneal Degeneration, Ribbonlike, with Deafness (C565157) ........Coxoauricular Syndrome (C565148) ........Davenport Donlan syndrome (C535988) ........Deaf-Blind Disorders (D054062) 26 ........Deafness hyperuricemia neurologic ataxia (C535995) ........Deafness with Labyrinthine Aplasia Microtia and Microdontia (LAMM) (C548011) ........DEAFNESS, AUTOSOMAL DOMINANT 22;DFNA22 DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY, (OMIM:606346) ........DEAFNESS, AUTOSOMAL DOMINANT 27 (OMIM:612431) ........DEAFNESS, AUTOSOMAL DOMINANT 33 (OMIM:614211) ........DEAFNESS, AUTOSOMAL DOMINANT 4A (OMIM:600652) ........DEAFNESS, AUTOSOMAL DOMINANT 50 (OMIM:613074) ........DEAFNESS, AUTOSOMAL DOMINANT 51 (OMIM:613558) ........DEAFNESS, AUTOSOMAL RECESSIVE 18A (OMIM:602092) ........DEAFNESS, AUTOSOMAL RECESSIVE 25 (OMIM:613285) ........DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT (OMIM:609006) ........DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT (OMIM:600791) ........DEAFNESS, AUTOSOMAL RECESSIVE 45 (OMIM:612433) ........DEAFNESS, AUTOSOMAL RECESSIVE 74 (OMIM:613718) ........DEAFNESS, AUTOSOMAL RECESSIVE 83 (OMIM:613685) ........DEAFNESS, AUTOSOMAL RECESSIVE 84A (OMIM:613391) ........DEAFNESS, AUTOSOMAL RECESSIVE 85 (OMIM:613392) ........DEAFNESS, AUTOSOMAL RECESSIVE 89 (OMIM:613916) ........DEAFNESS, AUTOSOMAL RECESSIVE 91 (OMIM:613453) ........Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities (C567467) ........Deafness, congenital onychodystrophy, recessive form (C538204) ........Deafness, Congenital, and Familial Myoclonic Epilepsy (C565649) ........Deafness, Congenital, and Onychodystrophy, Autosomal Dominant (C567274) ........Deafness, Congenital, with Vitiligo and Achalasia (C565642) ........DEAFNESS, NONSYNDROMIC, MODIFIER 1 (OMIM:605429) ........DEAFNESS, Y-LINKED 1 (OMIM:400043) ........Dementia, familial Danish (C538209) ........Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation (C566408) ........Emphysema, Congenital, With Deafness, Penoscrotal Web, And Mental Retardation (C566519) ........Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness (C565585) ........Fine-Lubinsky syndrome (C537933) ........Fountain syndrome (C537270) ........Herrmann syndrome (C538113) ........Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness (C565518) ........Hyperlipoproteinemia, Type II, and Deafness (C564170) ........HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS (OMIM:614187) ........Ichthyosiform erythroderma, corneal involvement, deafness (C537363) ........Johnson neuroectodermal syndrome (C535882) ........Jones syndrome (C535886) ........Keratitis, Ichthyosis, and Deafness (KID) Syndrome (C536168) ........Konigsmark Knox Hussels syndrome (C537214) ........Lynch Lee Murday syndrome (C537713) ........Mental retardation-hypotonic facies syndrome, x-linked, 1 (C537457) ........Meyenburg-Altherr-Uehlinger syndrome (C537574) ........Microcephaly deafness syndrome (C537326) ........MUCKLE-WELLS SYNDROME (OMIM:191900) ........MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500) ........Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders (C565786) ........Myoclonus, Cerebellar Ataxia, and Deafness (C563549) ........Nasodigitoacoustic syndrome (C538337) ........Nathalie syndrome (C538342) ........Nephrosis deafness urinary tract digital malformation (C536402) ........Noninsulin-dependent diabetes mellitus with deafness (C536246) ........Nonsyndromic Deafness (C580334) ........Opticocochleodentate Degeneration (C563002) ........PERRAULT SYNDROME 3 (OMIM:614129) ........Ramos Arroyo Clark syndrome (C535286) ........Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness (C567595) ........Richards-Rundle syndrome (C535674) ........Schimke X-linked mental retardation syndrome (C536630) ........Schlegelberger Grote syndrome (C536635) ........Secretory Diarrhea, Myopathy, and Deafness (C564382) ........Spastic paraplegia 24 (C536860) ........Temtamy preaxial brachydactyly syndrome (C536958) ........Tibia, Absence of, with Congenital Deafness (C564764) ........Tietz syndrome (C536919) ........Wells Jankovic syndrome (C536692) ........Wright Dyck syndrome (C536749) ........X-linked mental retardation Gustavson type (C536759) ........Yemenite deaf-blind hypopigmentation syndrome (C536771) Sister Nodes: ..Abidi X-linked mental retardation syndrome (C535556) ..Behr syndrome (C537669) ..Branchial arch syndrome X-linked (C537102) ..CATSHL syndrome (C537975) ..Chromosome 6pter-P24 Deletion Syndrome (C567239) ..Deafness (D003638) 108 ..Deafness with Anhidrotic Ectodermal Dysplasia (C565119) ..Deafness, Autosomal Dominant, Due To Mutation In Myo1a (C567266) ..Deafness, Autosomal Recessive 36, Without Vestibular Involvement (C567219) ..Deafness, Congenital Heart Defects, and Posterior Embryotoxon (C566604) ..Deafness, Unilateral, With Delayed Endolymphatic Hydrops (C567420) ..Deafness-Craniofacial Syndrome (C565118) ..Hearing Loss, Bilateral (D006312) 5 ..HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO (OMIM:613290) ..Hearing Loss, Conductive (D006314) 21 ..Hearing Loss, Functional (D006315) ..Hearing Loss, High-Frequency (D006316) ..Hearing Loss, Mixed Conductive-Sensorineural (D046089) 3 ..Hearing Loss, Sensorineural (D006319) 252 ..Hearing Loss, Sudden (D003639) ..Hearing Loss, Unilateral (D046088) 1 ..Iris dysplasia hypertelorism deafness (C535537) ..Lacrimoauriculodentodigital syndrome (C538132) ..Microcephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance (C567849) ..Microtia, Hearing Impairment, And Cleft Palate (C567359) ..Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay (C567769) ..Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant (C563497) ..Reardon Wilson Cavanagh syndrome (C535295) ..Spondylomegaepiphyseal Dysplasia With Upper Limb Mesomelia, Punctate Calcifications, And Deafness (C566507) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 2978
Name: Deafness
Definition: A general term for the complete loss of the ability to hear from both ears.
Alternative IDs:
ParentIDs: MESH:D034381
TreeNumbers: C09.218.458.341.186 |C10.597.751.418.341.186 |C23.888.592.763.393.341.186
Synonyms: Acquired Deafness |Bilateral Deafness |Complete Hearing Loss |Deaf Mutism |Deaf-Mutism |Deafness, Acquired |Deafness, Bilateral |Deafness, Prelingual |Extreme Hearing Loss |Hearing Loss, Complete |Hearing Loss, Extreme |Prelingual Deafness
Slim Mappings: Ear-nose-throat disease|Nervous system disease|Signs and symptoms
Reference:
MedGen: D003638
MeSH: D003638
OMIM: Genes: Could not execute query 3 SELECT DISTINCT t2.disease_id, t2.disease_title, t.id AS HPO_ID1, t.acc as HPO_ID, t.name as HPO_Name
, t5.frequency_modifier , o.comment AS Onset_name
FROM hpo.external_object_disease AS t2, hpo.annotation AS t5
LEFT JOIN hpo.term AS t ON t.id = t5.term_id
LEFT JOIN hpo.annotation_onset_modifier AS o ON o.annotation_id =t5.annotation_id
WHERE t2.disease_id = 'D003638' AND t2.db_name='OMIM'
AND t5.external_object_disease_id = t2.external_object_id
ORDER BY HPO_Name like '%Auto%' DESC, HPO_Name like '%linked%' DESC, HPO_Name like '%onset%' DESC, HPO_Name, disease_title, t.name;