acquired pseudoxanthoma elasticum
A nonheritable form of pseudoxanthoma elasticum (PXE), lacking the retinal and vascular stigmata associated with the inherited form of the disorder, but having skin lesions that are clinically, histologically, and ultrastructurally similar to those seen in the inherited type. [ PMID:528701 ]
Term info
- Orphanet:228247 (MONDO:equivalentTo)
- UMLS:C1274759 (Orphanet:228247/e)
- ICD9:757.39 (MONDO:relatedTo)
- SCTID:403401007 (MONDO:equivalentTo)
ordo_disease
A nonheritable form of pseudoxanthoma elasticum (PXE), lacking the retinal and vascular stigmata associated with the inherited form of the disorder, but having skin lesions that are clinically, histologically, and ultrastructurally similar to those seen in the inherited type.
http://purl.obolibrary.org/obo/Orphanet_228247, http://linkedlifedata.com/resource/umls/id/C1274759, http://identifiers.org/snomedct/403401007
acquired pseudoxanthoma elasticum, localized acquired cutaneous pseudoxanthoma elasticum, acquired PXE, acquired Gronblad-Strandberg-Touraine syndrome, acquired pseudoxanthoma elasticum (inherited or acquired)
MONDO:0016441