type I Ehlers-Danlos syndrome
Human disease
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type I Ehlers-Danlos syndrome
Summary
type I Ehlers-Danlos syndrome is a developmental defect during embryogenesis[1].
Key Facts
- type I Ehlers-Danlos syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- type I Ehlers-Danlos syndrome's instance of is recorded as class of disease[3].
- type I Ehlers-Danlos syndrome is a type of Ehlers-Danlos syndrome[4].
- type I Ehlers-Danlos syndrome is a type of autosomal dominant disease[5].
- type I Ehlers-Danlos syndrome's NCI Thesaurus ID is recorded as C125696[6].
- type I Ehlers-Danlos syndrome's genetic association is recorded as COL5A1[7].
- type I Ehlers-Danlos syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14720[8].
- type I Ehlers-Danlos syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14720[9].
- type I Ehlers-Danlos syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_90309[10].
- type I Ehlers-Danlos syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].