multiple synostoses syndrome 4

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Summary

Literature (0)

DOID:0081320 - multiple synostoses syndrome 4

Disease Ontology Definition:A multiple synostoses syndrome that is characterized by fusion of carpal and tarsal bones, as well as conductive hearing loss and that has_material_basis_in heterozygous mutation in the GDF6 gene on chromosome 8q22.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: gdf6

MIM:

MIM:617898 - MULTIPLE SYNOSTOSES SYNDROME 4; SYNS4

MIM:617898 - MULTIPLE SYNOSTOSES SYNDROME 4; SYNS4

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): multiple synostoses syndrome (is_a)