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Disease association ontology term - MONDO:0007369 - hereditary coproporphyria

Term summary

ID
MONDO:0007369
Name
hereditary coproporphyria
Ontology or CV name
Disease association
Definition
A form of acute hepatic porphyria characterized by the occurrence of neuro-visceral attacks and, more rarely, by the presence of cutaneous lesions.

Parents

Annotation

Disease association

MONDO:0007369 - hereditary coproporphyria

References:

Genes: