Fanconi renotubular syndrome 4

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Summary

Literature (0)

DOID:0080760 - Fanconi renotubular syndrome 4

Disease Ontology Definition:A Fanconi syndrome that has_material_basis_in heterozygous mutation in the HNF4A gene on chromosome 20q13.

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

: hnf4a

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

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

Parent(s): Fanconi syndrome (is_a), autosomal dominant disease (is_a)