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Disease association ontology term - MONDO:0037938 - inborn disorder of aspartate family metabolism

Term summary

ID
MONDO:0037938
Name
inborn disorder of aspartate family metabolism
Ontology or CV name
Disease association
Definition
An inherited metabolic disease that is has its basis in the disruption of aspartate family amino acid metabolic process.

Parents

Annotation

Disease association

MONDO:0100255 - adenosine kinase deficiency

References:

Genes:

MONDO:0000351 - disorder of methionine catabolism

References:

Genes:

MONDO:0009388 - hyperlysinemia

References:

Genes:

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

References:

Genes: