Fanconi renotubular syndrome 1

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Summary

Literature (0)

DOID:0080757 - Fanconi renotubular syndrome 1

Disease Ontology Definition:A Fanconi syndrome that has_material_basis_in heterozygous mutation in the GATM gene on chromosome 15q21.

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

MIM:

MIM:134600 - FANCONI RENOTUBULAR SYNDROME 1; FRTS1

MIM:134600 - FANCONI RENOTUBULAR SYNDROME 1; FRTS1

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

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

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