Disease association ontology term - MONDO:0013722 - hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism
Term summary
- ID
- MONDO:0013722
- Name
- hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism
- Ontology or CV name
- Disease association
- Definition
- Any leukodystrophy in which the cause of the disease is a mutation in the POLR3B gene.
