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DO Term : congenital malabsorptive diarrhea 4 [DOID:0060779] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital diarrhea characterized by chronic unremitting malabsorptive diarrhea and a profound dysgenesis of the enteroendocrine cells that has_material_basis_in mutation in the gene encoding neurogenin-3 (NEUROG3) on chromosome 10q21.3.

synonyms:
congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells,
OMIM:610370,
ICD10CM:P78.3,
congenital malabsorptive diarrhoea 4,
ORDO:83620,
enteric anendocrinosis,
610370,
congenital malabsorptive diarrhea due to paucity of enteroendocrine cells

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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