Disease association ontology term - MONDO:0030048 - harderoporphyria

Term summary

ID: MONDO:0030048
Name: harderoporphyria
Ontology or CV name: Disease association

Parents

is_a CPOX-related hereditary coproporphyria

Annotation

Disease association

MONDO:0030048 - harderoporphyria

References:

PB_REF:0000006

Genes:

hem13 (SPAC222.11)