# 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

**Wikidata**: [Q4357083](https://www.wikidata.org/wiki/Q4357083)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Galloway–Mowat_syndrome)  
**Source**: https://4ort.xyz/entity/galloway-mowat-syndrome


## References

1. [Source](https://ddrare.nibiohn.go.jp/)
2. Disease Ontology
3. Monarch Disease Ontology release 2018-06-29
4. Freebase Data Dumps. 2013
5. UniProt
6. Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndrome
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000177082/MONDO_0009627)
8. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000092094/MONDO_0009627)
9. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000172315/MONDO_0009627)
10. [Identifiers.org](https://registry.identifiers.org/registry/doid)