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DO Term : pancreatic agenesis 2 [DOID:0060988] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A pancreatic agenesis that has_material_basis_in homozygous or compound heterozygous mutation in a distal enhancer of the PTF1A gene on chromosome 10p12.

synonyms:
OMIM:615935,
615935

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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