Search Ontology:
Human Disease
Galloway-Mowat syndrome 10
- Term ID
- DOID:0061293
- Synonyms
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- Definition
- A Galloway-Mowat syndrome characterized by onset of symptoms soon after birth that has_material_basis_in homozygous or compound heterozygous mutation in the YRDC gene on chromosome 1p34. https://pubmed.ncbi.nlm.nih.gov/34545459/
- References
- Ontology
- Human Disease ( DOID:0061293 )
Other Pages
Genes Involved
Zebrafish Models