body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency is a very rare genetic skin disease characterized by severe skin laxity affecting the trunk and limbs. [ Orphanet:91135 ]
Term info
- Orphanet:91135 (OMIM:610842)
- MESH:C563654 (MONDO:equivalentTo)
- UMLS:C4049241 (MONDO:equivalentTo)
- SCTID:717941005 (MONDO:equivalentTo)
- OMIM:610842 (Orphanet:91135/e)
- UMLS:C1835813 (Orphanet:91135)
ordo_disease
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency is a very rare genetic skin disease characterized by severe skin laxity affecting the trunk and limbs.
http://identifiers.org/snomedct/717941005, http://purl.obolibrary.org/obo/Orphanet_91135, http://identifiers.org/mesh/C563654, http://linkedlifedata.com/resource/umls/id/C1835813, http://linkedlifedata.com/resource/umls/id/C4049241, https://omim.org/entry/610842
pseudoxanthoma elasticum-like syndrome, PXE-like syndrome
PXE-like disorder with multiple coagulation Factor deficiency, pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency
MONDO:0012570