Search Ontology:
Human Disease
congenital anomalies of the kidney and urinary tract 3
- Term ID
- DOID:0051078
- Synonyms
-
- Definition
- A congenital anomalies of the kidney and urinary tract that has_material_basis_in heterozygous mutation in the NRIP1 gene on chromosome 21q11-q21. https://pubmed.ncbi.nlm.nih.gov/28381549/
- References
- Ontology
- Human Disease ( DOID:0051078 )
Other Pages
Genes Involved
Zebrafish Models