ZFIN Human Disease: congenital malabsorptive diarrhea 4

OBO ID: DOID:0060779

Term Name:	congenital malabsorptive diarrhea 4		Search Ontology:
Synonyms:	congenital malabsorptive diarrhea due to paucity of enteroendocrine cells congenital malabsorptive diarrhoea 4 congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells enteric anendocrinosis
Definition:	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. https://www.ncbi.nlm.nih.gov/pubmed/16855267
References:	ICD10CM:P78.3 OMIM:610370 ORDO:83620
Ontology:	Human Disease ( DOID:0060779 )

Relationships

is a type of:	autosomal recessive disease congenital diarrhea autosomal recessive disease congenital diarrhea Show first 5 Terms

OTHER congenital malabsorptive diarrhea 4 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NEUROG3	neurog3	Diarrhea 4, malabsorptive, congenital	610370

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None