Galloway-Mowat syndrome 10
MONDO:0030476Mondo
Findings
No curated finding names Galloway-Mowat syndrome 10 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset · Infantile onset
HPO, annotations 2026-09-02
Features
15 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Congenital hypothyroidismHPOHP:0000851
- 3 of 3 reported patients · Congenital onset
- Delayed CNS myelinationHPOHP:0002188
- 2 of 2 reported patients
- Diffuse mesangial sclerosisHPOHP:0001967
- 2 of 2 reported patients
- MicrocephalyHPOHP:0000252
- 3 of 3 reported patients
- ProteinuriaHPOHP:0000093
- 3 of 3 reported patients
- Stage 5 chronic kidney diseaseHPOHP:0003774
- 3 of 3 reported patients · Infantile onset
- ArachnodactylyHPOHP:0001166
- 2 of 3 reported patients
- Secondary microcephalyHPOHP:0005484
- 2 of 3 reported patients
- Cerebellar atrophyHPOHP:0001272
- 1 of 2 reported patients
- Cerebral atrophyHPOHP:0002059
- 1 of 2 reported patients
- Podocyte foot process effacementHPOHP:0031266
- 1 of 2 reported patients
- Simplified gyral patternHPOHP:0009879
- 1 of 2 reported patients
Show the remaining 3
- HypotoniaHPOHP:0001252
- 1 of 3 reported patients
- MyoclonusHPOHP:0001336
- 1 of 3 reported patients
- Primary microcephalyHPOHP:0011451
- 1 of 3 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- YRDCHGNC:28905
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · G2P · Autosomal recessive · 2021
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
- A kind of
Other names
1 name
Resolves to: Galloway-Mowat syndrome 10
- Also called
- GAMOS10