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Summary Literature (0)
DOID:0111787 - frontometaphyseal dysplasia 2

Disease Ontology Definition:A frontometaphyseal dysplasia characterized by generalized skeletal dysplasia, deafness, urogenital defects and an increased tendency to form keloid scars that has_material_basis_in heterozygous mutation in MAP3K7 on chromosome 6q15.

Synonyms: FMD2

Xenbase Genes : map3k7


MIM:
MIM:617137 - FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), frontometaphyseal dysplasia (is_a)