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DO Term : poor metabolism of thiopurines [DOID:0080172] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An inherited metabolic disease that is characterized by significantly reduced activity of an enzyme that helps the body process drugs called thiopurines.

synonyms:
PS610460,
OMIM:PS610460,
TPMT deficiency,
MESH:C536512,
thiopurine S-methyltransferase deficiency

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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