Term Name:	frontometaphyseal dysplasia 2
Synonyms:	FMD2
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.
Ontology:	Human Disease [DOID:0111787]   ( DOID:0111787 )