Body skin hyperlaxity

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
BODY SKIN HYPERLAXITY DUE TO VITAMIN K DEPENDENT COAGULATION FACTOR DEFICIENCY
C4049241
GGCX Unknown — Disgenet
BODY SKIN HYPERLAXITY DUE TO VITAMIN K-DEPENDENT COAGULATION FACTOR DEFICIENCY
91135MONDO:0012570
GGCX Causal
17110937 24739904 28125048
ClinVar, GWAS catalog, Orphanet
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Body skin hyperlaxity.
5 View disease cluster →
Combined deficiency of vitamin k-dependent clotting factors 1 shared geneGGCX Related via 1 shared gene including GGCX. Blood coagulation disorder 1 shared geneGGCX Related via 1 shared gene including GGCX. Benign prostatic hyperplasia 1 shared geneGGCX Related via 1 shared gene including GGCX. Pulmonary arterial hypertension 1 shared geneGGCX Related via 1 shared gene including GGCX. Urolithiasis 1 shared geneGGCX Related via 1 shared gene including GGCX.