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Galloway-Mowat syndrome

rare

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

Identifiers
MONDO:0009627 Orphanet:2065
Part of
Autosomal recessive diseaseSyndromic disease
Also known as
cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities · Galloway Mowat syndrome · Galloway syndrome · GAMOS · hiatal hernia-microcephaly-nephrosis, Galloway type

Subtypes

All diseases Rare only
Disease Subtypes
Galloway-Mowat syndrome 1
Galloway-Mowat syndrome 10
Galloway-Mowat syndrome 2, X-linked
Galloway-Mowat syndrome 3
Galloway-Mowat syndrome 4
Galloway-Mowat syndrome 5
Galloway-Mowat syndrome 6
Galloway-Mowat syndrome 7
Galloway-Mowat syndrome 8
Galloway-Mowat syndrome 9

Rare disease

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