Galloway-Mowat syndrome (Q4357083)
Jump to navigation
Jump to search
autosomal recessive disease characterized by is a rare autosomal recessive disease, characterized by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome
- Galloway syndrome
- microcephaly, hiatal hernia and nephrotic syndrome
- nephrosis-microcephaly syndrome
- nephrosis-neuronal dysmigration syndrome
- Spinocerebellar ataxia, autosomal recessive 5
- GALLOWAY-MOWAT SYNDROME
- GAMOS
- Cerebellar Ataxia With Mental Retardation, Optic Atrophy, and Skin Abnormalities
- Microcephaly-hiatus hernia-nephrotic syndrome
- GALLOWAY-MOWAT SYNDROME; GAMOS
- Microcephaly, Hiatal Hernia, and Nephrotic Syndrome
- Spinocerebellar Ataxia, Autosomal Recessive 5, Formerly
- Galloway-Mowat syndrome 1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Galloway-Mowat syndrome |
autosomal recessive disease characterized by is a rare autosomal recessive disease, characterized by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome |
|
Statements
1 reference
17 May 2019
1 reference
1 reference
3 references
C132195
1 reference
C132195
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(5 entries)
- dewiki Galloway-Syndrom
- enwiki Galloway–Mowat syndrome
- fiwiki Galloway–Mowatin oireyhtymä
- plwiki Zespół Gallowaya-Mowata
- trwiki Galloway-Mowat sendromu