Ehlers-Danlos syndrome, dermatosparaxis type
human disease
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Ehlers-Danlos syndrome, dermatosparaxis type
Summary
Ehlers-Danlos syndrome, dermatosparaxis type is a developmental defect during embryogenesis[1].
Key Facts
- Ehlers-Danlos syndrome, dermatosparaxis type's instance of is recorded as developmental defect during embryogenesis[2].
- Ehlers-Danlos syndrome, dermatosparaxis type's instance of is recorded as rare disease[3].
- Ehlers-Danlos syndrome, dermatosparaxis type's instance of is recorded as class of disease[4].
- Ehlers-Danlos syndrome, dermatosparaxis type's subclass of is recorded as Ehlers-Danlos syndrome[5].
- Ehlers-Danlos syndrome, dermatosparaxis type's MeSH descriptor ID is recorded as C567527[6].
- Ehlers-Danlos syndrome, dermatosparaxis type's OMIM ID is recorded as 225410[7].
- Ehlers-Danlos syndrome, dermatosparaxis type's KEGG ID is recorded as H02244[8].
- Ehlers-Danlos syndrome, dermatosparaxis type's Orphanet ID is recorded as 1901[9].
- Ehlers-Danlos syndrome, dermatosparaxis type's genetic association is recorded as ADAMTS2[10].
- Ehlers-Danlos syndrome, dermatosparaxis type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1901[11].
- Ehlers-Danlos syndrome, dermatosparaxis type's UMLS CUI is recorded as C2700425[12].
- Ehlers-Danlos syndrome, dermatosparaxis type's ICD-10-CM is recorded as Q79.6[13].
- Ehlers-Danlos syndrome, dermatosparaxis type's GARD rare disease ID is recorded as 2089[14].
- Ehlers-Danlos syndrome, dermatosparaxis type's Mondo ID is recorded as MONDO_0009161[15].
- Ehlers-Danlos syndrome, dermatosparaxis type's ICD-11 ID is recorded as 445808781[16].
- Ehlers-Danlos syndrome, dermatosparaxis type's UniProt disease ID is recorded as DI-00444[17].