Gordon-Holmes syndrome
human disease
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Gordon-Holmes syndrome
Summary
Gordon-Holmes syndrome is a hereditary disorder[1]. It is known by 15 alternative names across languages and contexts.[2]
Key Facts
- Gordon-Holmes syndrome is credited with the discovery of Gordon Morgan Holmes[3].
- Gordon-Holmes syndrome's instance of is recorded as hereditary disorder[4].
- Gordon-Holmes syndrome's instance of is recorded as developmental defect during embryogenesis[5].
- Gordon-Holmes syndrome's instance of is recorded as rare disease[6].
- Gordon-Holmes syndrome's instance of is recorded as class of disease[7].
- Gordon-Holmes syndrome is a type of genetic movement disorder[8].
- Gordon-Holmes syndrome is a type of rare genetic developmental defect during embryogenesis[9].
- Gordon-Holmes syndrome is a type of autosomal recessive disease[10].
- Gordon-Holmes syndrome is a type of inherited metabolic disorder[11].
- Gordon-Holmes syndrome's NCI Thesaurus ID is recorded as C205640[12].
- Gordon-Holmes syndrome's genetic association is recorded as RNF216[13].
- Gordon-Holmes syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1173[14].
- Gordon-Holmes syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111587[15].
- Gordon-Holmes syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111587[16].
Body
Works and Contributions
Gordon-Holmes syndrome is credited with the discovery of Gordon Morgan Holmes[3].
Why It Matters
Gordon-Holmes syndrome is known by 15 alternative names across languages and contexts.[2]