Galloway-Mowat Syndrome

Alias:
Galloway Mowat Syndrome
Microcephaly-Hiatus Hernia-Nephrotic Syndrome
Nephrosis-Neuronal Dysmigration Syndrome
Galloway Syndrome
Microcephaly Hiatus Hernia Nephrotic Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Galloway-Mowat Syndrome, also known as galloway mowat syndrome, is related to galloway-mowat syndrome 1 and galloway-mowat syndrome 2. An important gene associated with Galloway-Mowat Syndrome is OSGEP (O-Sialoglycoprotein Endopeptidase), and among its related pathways/superpathways are Processing of Capped Intron-Containing Pre-mRNA and Gene Silencing by RNA. Affiliated tissues include brain and kidney, and related phenotypes are global developmental delay and microcephaly
Related ID:
MESH:C537548

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
XL
XLD
Newborn
--
60
314
1

Medical Symptom

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Description
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HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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MGI
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References Literature

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