split hand-foot malformation 6

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Summary

Literature (0)

DOID:0090026 - split hand-foot malformation 6

Disease Ontology Definition:A split-hand/foot malformation that has_material_basis_in homozygous mutation in the WNT10B gene on chromosome 12q13.

Synonyms: SHFM6,

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

: wnt10b

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009157 - split hand-foot malformation 6

MONDO:0009157 - split hand-foot malformation 6

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

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

Parent(s): autosomal recessive disease (is_a), split hand-foot malformation (is_a)