Human Disease and Mouse Model Detail
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Human Disease
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Porphyria, Acute Intermittent
OMIM ID: 176000
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Synonyms
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AIP;
PBGD Deficiency;
Porphobilinogen Deaminase Deficiency;
Porphyria, Swedish Type;
Uroporphyrinogen Synthase Deficiency
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View all models
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View ALL (1) mouse models for this human disease.
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Hmbs*
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HMBS*
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View 1 model
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1:1 Homology
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Mouse Models
Human Disease Modeled: Porphyria, Acute Intermittent
Associated Mouse Gene:
Hmbs
Analysis Tools