type III Ehlers-Danlos syndrome
Human disease
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type III Ehlers-Danlos syndrome
Summary
type III Ehlers-Danlos syndrome is a developmental defect during embryogenesis[1].
Key Facts
- type III Ehlers-Danlos syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- type III Ehlers-Danlos syndrome's instance of is recorded as class of disease[3].
- type III Ehlers-Danlos syndrome's subclass of is recorded as Ehlers-Danlos syndrome[4].
- type III Ehlers-Danlos syndrome's MeSH descriptor ID is recorded as C536196[5].
- type III Ehlers-Danlos syndrome's OMIM ID is recorded as 130020[6].
- type III Ehlers-Danlos syndrome's Disease Ontology ID is recorded as DOID:14757[7].
- type III Ehlers-Danlos syndrome's mode of inheritance is recorded as autosomal dominant[8].
- type III Ehlers-Danlos syndrome's Orphanet ID is recorded as 285[9].
- type III Ehlers-Danlos syndrome's NCI Thesaurus ID is recorded as C125698[10].
- type III Ehlers-Danlos syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14757[11].
- type III Ehlers-Danlos syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14757[12].
- type III Ehlers-Danlos syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_285[13].
- type III Ehlers-Danlos syndrome's UMLS CUI is recorded as C0268337[14].
- type III Ehlers-Danlos syndrome's ICD-10-CM is recorded as Q79.6[15].
- type III Ehlers-Danlos syndrome's GARD rare disease ID is recorded as 2081[16].
- type III Ehlers-Danlos syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- type III Ehlers-Danlos syndrome's Mondo ID is recorded as MONDO_0007523[18].
- type III Ehlers-Danlos syndrome's UniProt disease ID is recorded as DI-00438[19].