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DO Term : congenital secretory sodium diarrhea 3 [DOID:0060781] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13.

synonyms:
ORDO:103908,
OMIM:270420,
ICD10CM:P78.3,
270420,
congenital secretory sodium diarrhoea 3,
congenital secretory sodium diarrhea 3 with or without other congenital anomalies,
congenital secretory sodium diarrhea 3 syndromic,
congenital secretory sodium diarrhoea 3 with or without other congenital anomalies,
congenital secretory sodium diarrhoea 3 syndromic

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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