Search Ontology:
Human Disease
CAKUT1
- Term ID
- DOID:0080206
- Synonyms
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- Congenital anomalies of the kidney and urinary tract 1
- Definition
- A CAKUT that has_material_basis_in heterozygous mutation in the DSTYK gene on chromosome 1q32. https://www.ncbi.nlm.nih.gov/pubmed/23862974
- References
- Ontology
- Human Disease ( DOID:0080206 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models