FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term CAKUT2 ID (Ontology) DOID:0080207 (Human Disease)
Definition A CAKUT that has_material_basis_in heterozygous mutation in the TBX18 gene on chromosome 6q14.
Also Known As "Congenital anomalies of the kidney and urinary tract 2"
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 Genes
 CAKUT2       1
 for disease ribbon | CAKUT2       1
 model of | CAKUT2       1
Spanning Tree (Parents/Children)
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  urinary system disease
   |__CAKUT
       |__CAKUT2  1 rec.
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Synonyms
  • "Congenital anomalies of the kidney and urinary tract 2" EXACT
Secondary IDs
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MIM:143400