aplasia cutis congenita
http://purl.obolibrary.org/obo/MONDO_0007145
Aplasia cutis congenita (ACC) is a rare skin disorder characterized by localized absence of skin that is usually located on the scalp but can occur anywhere on the body including the face, trunk and extremities. ACC may occasionally be associated with other anomalies. [ Orphanet:1114 ]
Term info
- GARD:0000755 (MONDO:equivalentTo)
- ICD9:757.39 (MONDO:relatedTo)
- Orphanet:1114 (OMIM:107600)
- HP:0001057 (MONDO:otherHierarchy)
- OMIM:107600 (Orphanet:1114/e)
- NCIT:C98822 (MONDO:equivalentTo)
- GARD:0005835 (MONDO:equivalentTo)
- SCTID:35484002 (MONDO:equivalentTo)
gard_rare, ordo_malformation_syndrome
aplasia cutis congenita (disease)
Aplasia cutis congenita (ACC) is a rare skin disorder characterized by localized absence of skin that is usually located on the scalp but can occur anywhere on the body including the face, trunk and extremities. ACC may occasionally be associated with other anomalies.
http://purl.obolibrary.org/obo/Orphanet_1114, http://identifiers.org/snomedct/35484002, http://purl.obolibrary.org/obo/NCIT_C98822, https://omim.org/entry/107600
aplasia cutis congenita, aplasia cutis congenita (disease), aplasia cutis congenita recessive
ACC, scalp defect, congenital, congenital defect of skull and scalp, aplasia cutis congenita nonsyndromic, scalp defect congenital, aplasia cutis congenita, nonsyndromic
MONDO:0007145