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 is a type of Ehlers-Danlos syndrome[5].
- Ehlers-Danlos syndrome, dermatosparaxis type's genetic association is recorded as ADAMTS2[6].
- Ehlers-Danlos syndrome, dermatosparaxis type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1901[7].