About: congenital diarrhea 7 with exudative enteropathy

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal recessive disease congenital diarrhea nodeID://b50939369 nodeID://b50939370 nodeID://b50939371
label	congenital diarrhea 7 with exudative enteropathy
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060778
database_cross_reference	ICD10CM:P78.3 OMIM:615863 ORDO:329242
has_exact_synonym	congenital chronic diarrhoea with protein-losing enteropathy (en) congenital diarrhoea 7 with exudative enteropathy (en) congenital chronic diarrhea with exudative enteropathy (en) congenital chronic diarrhea with protein-losing enteropathy (en) congenital chronic diarrhoea with exudative enteropathy (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A congenital diarrhea characterized by watery diarrhea, protein-losing enteropathy, patchy areas of dystrophic microvilli in the duodenum and patchy areas of villous atrophy that has_material_basis_in homozygous mutation in the DGAT1 gene on chromosome 8q24.3.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50939372

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