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DO Term : frontometaphyseal dysplasia 2 [DOID:0111787] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • 617137,
  • FMD2,
  • OMIM:617137
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents