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    Disease Ontology Term: renal cysts and diabetes syndrome


    DO ID
    DOID:0111101
    Description
    A maturity-onset diabetes of the young characterized by abnormal renal development resuting in non-diabetic kidney disease and diabetes that has_material_basis_in mutation in the HNF1B gene on chromosome 17q12.
    Synonyms
    atypical familial juvenile hyperuricemic nephropathy, atypical FJHN, CAKUT with diabetes, congenital anomalies of the kidney and urinary tract with diabetes, familial hypoplastic glomerulocystic kidney, hypoplastic type glomerulocystic kidney disease, maturity-onset diabetes of the young type 5, MODY5, RCAD
    View DO Annotations for yeast and other model organisms at the Alliance of Genome Resources

    Ontology Diagram


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    Evidence ID Analyze ID Gene Gene Systematic Name Disease Ontology Term Disease Ontology Term ID Qualifier Evidence Method Source Assigned On Reference
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    Evidence ID Analyze ID Gene Gene Systematic Name Disease Ontology Term Disease Ontology Term ID Qualifier Evidence Method Source Assigned On Reference
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    Evidence ID Analyze ID Gene Gene Systematic Name Disease Ontology Term Disease Ontology Term ID Qualifier Evidence Method Source Assigned On Reference
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