has material basis in germline mutation in disease arises from feature disease has basis in feature disease shares features of GGCX Abnormality of coagulation body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency https://github.com/monarch-initiative/mondo/issues/6749 https://www.malacards.org/card/body_skin_hyperlaxity_due_to_vitamin_k_dependent_coagulation_factor_deficiency https://www.malacards.org/card/pseudoxanthoma_elasticum_like_disorder_with_multiple_coagulation_factor_deficiency MONDO:0012570 PXE-like syndrome GARD:0016796 MESH:C563654 SCTID:717941005 OMIM:610842 UMLS:C1835813 MEDGEN:332067 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 pseudoxanthoma elasticum-like syndrome pseudoxanthoma elasticum (inherited or acquired) hereditary skin disorder