Disease #05269 (OSFD (dysplasia, osteofibrous, susceptibility to (OSFD)), OMIM:607278)

Official abbreviation OSFD
Name dysplasia, osteofibrous, susceptibility to (OSFD)
OMIM ID 607278
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MET
Associated tissues -
Disease features -
Remarks -