syndromic genetic deafness
human disease
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syndromic genetic deafness
Summary
syndromic genetic deafness is a head and neck disease[1].
Key Facts
- syndromic genetic deafness's instance of is recorded as head and neck disease[2].
- syndromic genetic deafness's instance of is recorded as developmental defect during embryogenesis[3].
- syndromic genetic deafness's instance of is recorded as class of disease[4].
- syndromic genetic deafness's subclass of is recorded as rare genetic developmental defect during embryogenesis[5].
- syndromic genetic deafness's subclass of is recorded as rare deafness[6].
- syndromic genetic deafness's subclass of is recorded as developmental defect during embryogenesis[7].
- syndromic genetic deafness's subclass of is recorded as genetic deafness[8].
- syndromic genetic deafness's Orphanet ID is recorded as 90642[9].
- syndromic genetic deafness's genetic association is recorded as GJB2[10].
- syndromic genetic deafness's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_90642[11].
- syndromic genetic deafness's UMLS CUI is recorded as C0395976[12].
- syndromic genetic deafness's ICD-10-CM is recorded as H90.3[13].
- syndromic genetic deafness's on focus list of Wikimedia project is recorded as WikiProject Hearing Health[14].
- syndromic genetic deafness's Mondo ID is recorded as MONDO_0019589[15].
- syndromic genetic deafness's ICD-11 ID is recorded as LD2H[16].
- syndromic genetic deafness's ICD-11 ID is recorded as 186534168[17].
- syndromic genetic deafness's KBpedia ID is recorded as SyndromicGeneticDeafness[18].