Search Ontology:
Human Disease
Galloway-Mowat syndrome 4
- Term ID
- DOID:0080246
- Synonyms
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- Definition
- A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TP53RK gene on chromosome 20q13. https://pubmed.ncbi.nlm.nih.gov/28805828/
- References
- Ontology
- Human Disease ( DOID:0080246 )
- is a type of
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