Galloway-Mowat syndrome

MONDO:0009627

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

Also known as: 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

0 clinical trials for this condition and its sub-types, 0 tagged with Galloway-Mowat syndrome itself.

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↑ Syndromic disease (7133) ↑ Autosomal recessive disease (994)

Sub-types of Galloway-Mowat syndrome

Galloway-Mowat syndrome 1 0 trials
Galloway-Mowat syndrome 10 0 trials
Galloway-Mowat syndrome 2, X-linked 0 trials
Galloway-Mowat syndrome 3 0 trials
Galloway-Mowat syndrome 4 0 trials
Galloway-Mowat syndrome 5 0 trials
Galloway-Mowat syndrome 6 0 trials
Galloway-Mowat syndrome 7 0 trials
Galloway-Mowat syndrome 8 0 trials
Galloway-Mowat syndrome 9 0 trials

Including sub-types (0) Tagged with Galloway-Mowat syndrome (0)

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