cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 2

Summary

DOID:0070557 - cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 2

Disease Ontology Definition:A cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome that has_material_basis_in homozygous mutation in the WDR81 gene on chromosome 17p13.3.

Synonyms: CAMRQ syndrome 2, CAMRQ2, cerebellar ataxia and mental retardation with or without quadrupedal locomotion 2, cerebellar ataxia, mental retardation, and disequilibrium syndrome 2, cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2

Echinobase 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

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

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

Parent(s): cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome (is_a)