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's subclass of is recorded as Ehlers-Danlos syndrome[4].
- type I Ehlers-Danlos syndrome's subclass of is recorded as autosomal dominant disease[5].
- type I Ehlers-Danlos syndrome's MeSH descriptor ID is recorded as C536194[6].
- type I Ehlers-Danlos syndrome's OMIM ID is recorded as 130000[7].
- type I Ehlers-Danlos syndrome's Disease Ontology ID is recorded as DOID:14720[8].
- type I Ehlers-Danlos syndrome's Orphanet ID is recorded as 287[9].
- type I Ehlers-Danlos syndrome's Orphanet ID is recorded as 90309[10].
- type I Ehlers-Danlos syndrome's NCI Thesaurus ID is recorded as C125696[11].
- type I Ehlers-Danlos syndrome's genetic association is recorded as COL5A1[12].
- type I Ehlers-Danlos syndrome's Google Knowledge Graph ID is recorded as /g/122v8ndf[13].
- type I Ehlers-Danlos syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14720[14].
- type I Ehlers-Danlos syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14720[15].
- type I Ehlers-Danlos syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_90309[16].
- type I Ehlers-Danlos syndrome's UMLS CUI is recorded as C0268335[17].
- type I Ehlers-Danlos syndrome's UMLS CUI is recorded as C4225429[18].
- type I Ehlers-Danlos syndrome's ICD-10-CM is recorded as Q79.6[19].
- type I Ehlers-Danlos syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
- type I Ehlers-Danlos syndrome's Mondo ID is recorded as MONDO_0019567[21].
- type I Ehlers-Danlos syndrome's ICD-11 ID is recorded as 1999142975[22].
- type I Ehlers-Danlos syndrome's UniProt disease ID is recorded as DI-00436[23].