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Disease association ontology term - MONDO:0010212 - xeroderma pigmentosum group D

Term summary

ID
MONDO:0010212
Name
xeroderma pigmentosum group D
Ontology or CV name
Disease association
Definition
Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC2 gene.

Parents

Annotation

Disease association

MONDO:0010212 - xeroderma pigmentosum group D

References:

Genes: