Markedly decreased coproporphyrinogen oxidase activity (harderoporphyria, lymphocytes)

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Markedly decreased coproporphyrinogen oxidase activity (harderoporphyria, lymphocytes)" [OMIM:Markedly decreased coproporphyrinogen oxidase activity (harderoporphyria, lymphocytes)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Hereditary coproporphyria (Orphanet:79273)