Search Ontology:
Human Disease

CAKUT1

Term ID
DOID:0080206
Synonyms
  • 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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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