Harboyan syndrome
human disease
Press Enter · cited answer in seconds
0 sources
Harboyan syndrome
Summary
Harboyan syndrome is a head and neck disease[1]. It draws 6 Wikipedia views per month (head_and_neck_disease category, ranking #54 of 92).[2]
Key Facts
- Harboyan syndrome's instance of is recorded as head and neck disease[3].
- Harboyan syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Harboyan syndrome's instance of is recorded as rare disease[5].
- Harboyan syndrome's instance of is recorded as class of disease[6].
- Harboyan syndrome's subclass of is recorded as corneal dystrophy[7].
- Harboyan syndrome's subclass of is recorded as genetic deafness[8].
- Harboyan syndrome's subclass of is recorded as syndromic genetic deafness[9].
- Harboyan syndrome's subclass of is recorded as syndromic corneal dystrophy[10].
- Harboyan syndrome's subclass of is recorded as autosomal recessive disease[11].
- Harboyan syndrome's subclass of is recorded as syndrome[12].
- Harboyan syndrome's Commons category is recorded as Harboyan syndrome[13].
- Harboyan syndrome's MeSH descriptor ID is recorded as C535473[14].
- Harboyan syndrome's OMIM ID is recorded as 217400[15].
- Harboyan syndrome's Disease Ontology ID is recorded as DOID:0111620[16].
- Harboyan syndrome's Orphanet ID is recorded as 1490[17].
- Harboyan syndrome's genetic association is recorded as SLC4A11[18].
- Harboyan syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1490[19].
- Harboyan syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111620[20].
- Harboyan syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111620[21].
- Harboyan syndrome's UMLS CUI is recorded as C1857572[22].
- Harboyan syndrome's ICD-10-CM is recorded as H18.5[23].
- Harboyan syndrome's GARD rare disease ID is recorded as 1529[24].
- Harboyan syndrome's Mondo ID is recorded as MONDO_0009015[25].
- Harboyan syndrome's ICD-11 ID is recorded as 1379977650[26].
- Harboyan syndrome's WikiProjectMed ID is recorded as Corneal dystrophy-perceptive deafness syndrome[27].
Why It Matters
Harboyan syndrome draws 6 Wikipedia views per month (head_and_neck_disease category, ranking #54 of 92).[2]