PomBase home

Disease association ontology term - MONDO:0014384 - hypotrichosis 12

Term summary

ID
MONDO:0014384
Name
hypotrichosis 12
Ontology or CV name
Disease association
Definition
Any hypotrichosis in which the cause of the disease is a mutation in the RPL21 gene.

Parents

Annotation

Disease association

MONDO:0014384 - hypotrichosis 12

References:

Genes: