Harboyan syndrome
human disease
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Harboyan syndrome
Summary
Harboyan syndrome is a head and neck disease[1].
Key Facts
- Harboyan syndrome's instance of is recorded as head and neck disease[2].
- Harboyan syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Harboyan syndrome's instance of is recorded as rare disease[4].
- Harboyan syndrome's instance of is recorded as class of disease[5].
- Harboyan syndrome is a type of corneal dystrophy[6].
- Harboyan syndrome is a type of genetic deafness[7].
- Harboyan syndrome is a type of syndromic genetic deafness[8].
- Harboyan syndrome is a type of syndromic corneal dystrophy[9].
- Harboyan syndrome is a type of autosomal recessive disease[10].
- Harboyan syndrome is a type of syndrome[11].
- Harboyan syndrome's Commons category is recorded as Harboyan syndrome[12].
- Harboyan syndrome's genetic association is recorded as SLC4A11[13].
- Harboyan syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1490[14].
- Harboyan syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111620[15].
- Harboyan syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111620[16].