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Disease association ontology term - MONDO:0014669 - cone-rod dystrophy 21

Term summary

ID
MONDO:0014669
Name
cone-rod dystrophy 21
Ontology or CV name
Disease association
Definition
Any cone-rod dystrophy in which the cause of the disease is a mutation in the DRAM2 gene.

Parents

Annotation

Disease association

MONDO:0014669 - cone-rod dystrophy 21

References:

Genes: