OBO ID: DOID:0080207
Term Name: CAKUT2 Search Ontology:
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 CAKUT2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TBX18 Congenital anomalies of kidney and urinary tract 2 143400
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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