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Winchester syndrome

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Uniprot Description A disease characterized by severe osteolysis in the hands and feet, generalized osteoporosis, bone thinning, and absence of subcutaneous nodules. Various additional features include coarse face, corneal opacities, gum hypertrophy, and EKG changes.
Mondo Term and Equivalent IDs
MONDO:0010201:  Winchester syndrome
GARD:0007894: 
SCTID:254151006: 
UMLS:CN204453: