PomBase home

Disease association ontology term - MONDO:0008296 - familial porphyria cutanea tarda

Term summary

ID
MONDO:0008296
Name
familial porphyria cutanea tarda
Ontology or CV name
Disease association
Definition
An instance of porphyria cutanea tarda that is caused by an inherited modification of the individual's genome.

Parents

Annotation

Disease association

MONDO:0008296 - familial porphyria cutanea tarda

References:

Genes: