PomBase home

Disease association ontology term - MONDO:0017356 - inborn disorder of ornithine metabolism

Term summary

ID
MONDO:0017356
Name
inborn disorder of ornithine metabolism
Ontology or CV name
Disease association
Definition
An inherited metabolic disease that is has its basis in the disruption of ornithine metabolic process.

Parents

Annotation

Disease association

MONDO:0009053 - ALDH18A1-related de Barsy syndrome

References:

Genes:

MONDO:0014702 - autosomal recessive complex spastic paraplegia type 9B

References:

Genes:

MONDO:0014706 - cutis laxa, autosomal dominant 3

References:

Genes:

MONDO:0011006 - hereditary spastic paraplegia 9A

References:

Genes:

MONDO:0009796 - ornithine aminotransferase deficiency

References:

Genes: