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Disease association ontology term - MONDO:0014466 - Neu-Laxova syndrome 2

Term summary

ID
MONDO:0014466
Name
Neu-Laxova syndrome 2
Ontology or CV name
Disease association
Definition
Any Neu-Laxova syndrome in which the cause of the disease is a mutation in the PSAT1 gene.

Parents

Annotation

Disease association

MONDO:0014466 - Neu-Laxova syndrome 2

References:

Genes: