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Galloway-Mowat Syndrome (MONDO:0009627)

Open Trait in OLS

Galloway syndrome is characterized by the association of nephrotic syndrome and central nervous system anomalies.

Overview

Category

syndromic disease

Ontology ID

MONDO:0009627

Internal:10847

Synonyms

Galloway syndrome

Galloway-Mowat syndrome

microcephaly, hiatal hernia and nephrotic syndrome

microcephaly-hiatus hernia-nephrotic syndrome

nephrosis-microcephaly syndrome

nephrosis-neuronal dysmigration syndrome

spinocerebellar ataxia, autosomal recessive 5

GAMOS

Galloway Mowat syndrome

cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities

cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities

hiatal hernia-microcephaly-nephrosis, Galloway type

microcephaly nephrosis syndrome

microcephaly, hiatal hernia, and nephrotic syndrome

nephrosis neuronal dysmigration syndrome

spinocerebellar ataxia, autosomal recessive 5, formerly

Mapped terms

DOID:0080694

GARD:0000065

MEDGEN:167086

MESH:C537548

NANDO:1200713

NANDO:2200120

NANDO:2201385

NCIT:C132195

NORD:1171

OMIMPS:251300

Orphanet:2065

SCTID:721297008

UMLS:C0795949

Child terms

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