Ehlers-Danlos syndrome type 2
human disease
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Ehlers-Danlos syndrome type 2
Summary
Ehlers-Danlos syndrome type 2 is a developmental defect during embryogenesis[1].
Key Facts
- Ehlers-Danlos syndrome type 2's instance of is recorded as developmental defect during embryogenesis[2].
- Ehlers-Danlos syndrome type 2's instance of is recorded as class of disease[3].
- Ehlers-Danlos syndrome type 2's subclass of is recorded as type I Ehlers-Danlos syndrome[4].
- Ehlers-Danlos syndrome type 2's said to be the same as is recorded as type I Ehlers-Danlos syndrome[5].
- Ehlers-Danlos syndrome type 2's MeSH descriptor ID is recorded as C536195[6].
- Ehlers-Danlos syndrome type 2's Orphanet ID is recorded as 90318[7].
- Ehlers-Danlos syndrome type 2's NCI Thesaurus ID is recorded as C125697[8].
- Ehlers-Danlos syndrome type 2's genetic association is recorded as COL5A2[9].
- Ehlers-Danlos syndrome type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_90318[10].
- Ehlers-Danlos syndrome type 2's UMLS CUI is recorded as C0268336[11].
- Ehlers-Danlos syndrome type 2's ICD-10-CM is recorded as Q79.6[12].
- Ehlers-Danlos syndrome type 2's Mondo ID is recorded as MONDO_0019568[13].
- Ehlers-Danlos syndrome type 2's ICD-11 ID is recorded as 1973837258[14].