Disease

Galloway-Mowat syndrome 1

Name: Galloway-Mowat syndrome 1
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0060364 Galloway-Mowat syndrome 1 A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25. Galloway syndrome nephrosis-microcephaly syndrome SCAR5 microcephaly, hiatal hernia and nephrotic syndrome autosomal recessive spinocerebellar ataxia 5 nephrosis-neuronal dysmigration syndrome

Definition

A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25.

Synonyms

autosomal recessive spinocerebellar ataxia 5
Galloway syndrome

Cross References

MIM:251300

Parent Terms

autosomal recessive disease
Galloway-Mowat syndrome

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

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Associated Alleles

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Associated Models

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