syndromic genetic deafness
human disease
Press Enter · cited answer in seconds
0 sources
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 is a type of rare genetic developmental defect during embryogenesis[5].
- syndromic genetic deafness is a type of rare deafness[6].
- syndromic genetic deafness is a type of developmental defect during embryogenesis[7].
- syndromic genetic deafness is a type of genetic deafness[8].
- syndromic genetic deafness's genetic association is recorded as GJB2[9].
- syndromic genetic deafness's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_90642[10].
- syndromic genetic deafness's on focus list of Wikimedia project is recorded as WikiProject Hearing Health[11].