Disease association ontology term - MONDO:0000351 - disorder of methionine catabolism

Term summary

ID: MONDO:0000351
Name: disorder of methionine catabolism
Ontology or CV name: Disease association
Definition: An inherited metabolic disease that is has its basis in the disruption of methionine catabolic process.

Parents

is_a inborn disorder of amino acid metabolism
is_a inborn disorder of methionine cycle and sulfur amino acid metabolism
is_a inborn disorder of aspartate family metabolism

Annotation

Disease association

MONDO:0000351 - disorder of methionine catabolism

References:

PB_REF:0000003

Genes:

MONDO:0100255 - adenosine kinase deficiency

References:

PB_REF:0000006

Genes:

ado1 (SPCC338.14)

MONDO:0013404 - hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase

References:

PB_REF:0000006

Genes:

sah1 (SPBC8D2.18c)