Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandCongenital Abnormalities (D000013)
..Starting node
..expandAbnormalities, Drug-Induced (D000014)

       Child Nodes:
........expandAccutane embryopathy (C535670)
........expandAcitretin embryopathy (C538169)
........expandFetal hydantoin syndrome (C537922)
........expandFetal trimethadione syndrome (C537798)
........expandHo Kaufman Mcalister syndrome (C538325)
........expandIsotretinoin embryopathy like syndrome (C535542)
........expandValproic acid antenatal infection (C536525)
........expandWarfarin syndrome (C536683)



 Sister Nodes: 
..expandAbnormalities, Drug-Induced (D000014) Child8
..expandAbnormalities, Multiple (D000015) Child715
..expandAbnormalities, Radiation-Induced (D000016)
..expandAbnormalities, Severe Teratoid (D009008) Child6
..expandAbsent breasts and nipples (C535565)
..expandAccessory pancreas (C536003)
..expandAICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency (C563876)
..expandAicardi Syndrome (D058540) Child1
..expandArrhinia (C537438)
..expandAtlanto-Axial Fusion (C538196)
..expandAural Atresia, Congenital (C564321)
..expandBile and Pancreatic Ducts, Complete Absence of (C564298)
..expandBrain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear/Eye Anomalies, Cleft Palate/Cryptorchidism, And (C564519)
..expandCardiovascular Abnormalities (D018376) Child331
..expandCaudal Duplication Anomaly (C564315)
..expandChromosome Disorders (D025063) Child160
..expandCongenital Microtia (D065817) Child12
..expandCrane-Heise syndrome (C536452)
..expandCryptotia, Familial (C565140)
..expandDeal Barratt Dillon syndrome (C538206)
..expandDigestive System Abnormalities (D004065) Child78
..expandEye Abnormalities (D005124) Child208
..expandGallbladder, Agenesis Of (C562564)
..expandHereditary renal agenesis (C536482)
..expandHernias, Diaphragmatic, Congenital (D065630) Child7
..expandHydrocephalus, Skeletal Anomalies, and Mental Disturbance (C563413)
..expandLaryngeal cleft (C537875)
..expandLaryngeal Web, Familial (C563636)
..expandLymphatic Abnormalities (D044148) Child10
..expandMullerian aplasia (C537371) Child1
..expandMusculoskeletal Abnormalities (D009139) Child1165
..expandNasal Bones, Absence of (C562753)
..expandNervous System Malformations (D009421) Child567
..expandPancreas agenesis, dorsal (C538109)
..expandPatterson Stevenson syndrome (C536311) Child1
..expandRenal and Mullerian Duct Hypoplasia (C564853)
..expandRespiratory System Abnormalities (D015619) Child27
..expandRhiny (C566708)
..expandSaito Kuba Tsuruta syndrome (C537226)
..expandSchlegelberger Grote syndrome (C536635)
..expandSitus Inversus (D012857) Child19
..expandSkin Abnormalities (D012868) Child358
..expandSprengel deformity (C535802)
..expandStomatognathic System Abnormalities (D018640) Child329
..expandStridor, Congenital (C563163)
..expandThyroid Dysgenesis (D050033) Child3
..expandUrogenital Abnormalities (D014564) Child196
..expandVagina, absence of (C536523)
..expandVertebral fusion posterior lumbosacral blepharoptosis (C536344)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:83
Name:Abnormalities, Drug-Induced
Definition:Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently exposed during the manufacture of such substances. The concept excludes abnormalities resulting from exposure to non-medicinal chemicals in the environment.
Alternative IDs:
ParentIDs:MESH:D000013
TreeNumbers:C16.131.042
Synonyms:Abnormalities, Drug Induced |Abnormality, Drug-Induced |Drug Induced Abnormalities |Drug-Induced Abnormalities |Drug-Induced Abnormality
Slim Mappings:Congenital abnormality
Reference: MedGen: D000014
MeSH: D000014
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants