Search Ontology:
Human Disease

CAKUT2

Term ID
DOID:0080207
Synonyms
  • Congenital anomalies of the kidney and urinary tract 2
Definition
A CAKUT that has_material_basis_in heterozygous mutation in the TBX18 gene on chromosome 6q14. https://www.ncbi.nlm.nih.gov/pubmed/26235987
References
Ontology
Human Disease   ( DOID:0080207 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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