FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term congenital diarrhea 6 ID (Ontology) DOID:0060780 (Human Disease)
Definition A congenital diarrhea characterized by mild, early-onset chronic diarrhea that has_material_basis_in heterozygous mutation in the GUCY2C gene on chromosome 12p12.
Also Known As "chronic diarrhea due to guanylate cyclase 2C overactivity" ; "chronic diarrhoea due to guanylate cyclase 2C overactivity" ; "congenital diarrhoea 6"
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 Genes
 congenital diarrhea 6       1
 for disease ribbon | congenital diarrhea 6       1
 model of | congenital diarrhea 6       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
physical disorder               |
 |__congenital diarrhea_________|
diarrhea                        |
 |__congenital diarrhea_________|
                                congenital diarrhea 6  1 rec.
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Is a autosomal dominant disease
congenital diarrhea
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Synonyms
  • "chronic diarrhea due to guanylate cyclase 2C overactivity" EXACT
    "chronic diarrhoea due to guanylate cyclase 2C overactivity" EXACT
    "congenital diarrhoea 6" EXACT
Secondary IDs
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ICD10CM:P78.3
MIM:614616
ORDO:314373