Disease Browser            Parent Node: Hearing Disorders (D006311) ..Starting node ..Hearing Loss (D034381)        Child 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)  Sister Nodes:  ..Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia (C580009) ..Hearing Loss (D034381) 397 ..Hyperacusis (D012001) ..Ossicular Malformations, familial (C537142) ..Tinnitus (D014012) 1     Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

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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 = 'D034381' 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;

Term ID:	4921
Name:	Hearing Loss
Definition:	A general term for the complete or partial loss of the ability to hear from one or both ears.
Alternative IDs:
ParentIDs:	MESH:D006311
TreeNumbers:	C09.218.458.341 |C10.597.751.418.341 |C23.888.592.763.393.341
Synonyms:	Hearing Impairment |Hypoacuses |Hypoacusis |Loss, Hearing
Slim Mappings:	Ear-nose-throat disease|Nervous system disease|Signs and symptoms
Reference:	MedGen: D034381 MeSH: D034381 OMIM: Genes: