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osteopoikilosis

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description A rare autosomal dominant inherited disorder characterized by the presence of small areas of increased density throughout the bones.
Disease Ontology Description An osteosclerosis that results_in numerous bone islands located_in skeleton.
Mondo Term and Equivalent IDs
MONDO:0001414:  osteopoikilosis
GARD:0004158: 
ICD9:756.53: 
MESH:D010023: 
NCIT:C84985: 
SCTID:9147009: