wrinkly skin syndrome
medical condition
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Summary
wrinkly skin syndrome is a developmental defect during embryogenesis[1].
Key Facts
- wrinkly skin syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- wrinkly skin syndrome's instance of is recorded as rare disease[3].
- wrinkly skin syndrome's instance of is recorded as class of disease[4].
- wrinkly skin syndrome is a type of cutis laxa[5].
- wrinkly skin syndrome is a type of autosomal recessive disease[6].
- wrinkly skin syndrome is a type of syndrome[7].
- wrinkly skin syndrome's ICD-9-CM is recorded as 259.8[8].
- wrinkly skin syndrome's health specialty is recorded as rheumatology[9].
- wrinkly skin syndrome's health specialty is recorded as dermatology[10].
- wrinkly skin syndrome's genetic association is recorded as ATP6V0A2[11].
- wrinkly skin syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2834[12].
- wrinkly skin syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_357058[13].
- wrinkly skin syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0112171[14].
- wrinkly skin syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0112171[15].