Erythrocyte porphobilinogen (PBG) deaminase deficiency (exception: type II AIP)

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Erythrocyte porphobilinogen (PBG) deaminase deficiency (exception: type II AIP)" [OMIM:Erythrocyte porphobilinogen (PBG) deaminase deficiency (exception: type II AIP)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Acute intermittent porphyria (Orphanet:79276)