acrogeria
A congenital skin condition characterized by premature aging, more especially in the form of unusually fragile, thin skin on the hands and feet. Its onset is in early childhood; it progresses over the next few years and then remains stable. A bruising tendency has been observed. [ Wikipedia:Acrogeria ]
Term info
- MESH:C538187 (Orphanet:2500/e)
- ICD9:259.8 (MONDO:relatedTo)
- UMLS:C0406584 (Orphanet:2500/e)
- Orphanet:2500 (OMIM:201200)
- UMLS:C0238590 (Orphanet:2500/e)
- GARD:0006543 (MONDO:equivalentTo)
- SCTID:238872007 (MONDO:equivalentTo)
- OMIM:201200 (Orphanet:2500/e)
ordo_malformation_syndrome
A congenital skin condition characterized by premature aging, more especially in the form of unusually fragile, thin skin on the hands and feet. Its onset is in early childhood; it progresses over the next few years and then remains stable. A bruising tendency has been observed.
http://purl.obolibrary.org/obo/Orphanet_2500, http://linkedlifedata.com/resource/umls/id/C0406584, https://omim.org/entry/201200, http://identifiers.org/mesh/C538187, http://linkedlifedata.com/resource/umls/id/C0238590, http://identifiers.org/snomedct/238872007
acrogeria, Gottron type, Gottron syndrome, acrometageria
familial acrogeria, Metageria
MONDO:0008716