All diseases

OMIM ID
176000
OMIM term:
PORPHYRIA, ACUTE INTERMITTENT
Alternative terms:
AIP
PORPHYRIA, SWEDISH TYPE
PORPHOBILINOGEN DEAMINASE DEFICIENCY
PBGD DEFICIENCY
UROPORPHYRINOGEN SYNTHASE DEFICIENCY
UPS DEFICIENCY PORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED
PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED
(∗) Location:
11q23.3  
(†) Associated OMIM genes:
HMBS  
(‡) Associated MGI genes:
Hmbs  

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