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MeSH Tree Location(s) for Porphyria, Acute Intermittent

Scope Note:
An autosomal dominant porphyria that is due to a deficiency of HYDROXYMETHYLBILANE SYNTHASE in the LIVER, the third enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features are recurrent and life-threatening neurologic disturbances, ABDOMINAL PAIN, and elevated level of AMINOLEVULINIC ACID and PORPHOBILINOGEN in the urine.

See also: Hydroxymethylbilane Synthase


Location corresponding to Mesh Number C06.552.830.150

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Acute Intermittent   Porfyri, akut intermittent
Location corresponding to Mesh Number C16.320.565.708.400.150

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Acute Intermittent   Porfyri, akut intermittent
Location corresponding to Mesh Number C16.320.850.742.150

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Acute Intermittent   Porfyri, akut intermittent
Location corresponding to Mesh Number C17.800.827.742.150

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Acute Intermittent   Porfyri, akut intermittent
Location corresponding to Mesh Number C17.800.849.617.400.150

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Acute Intermittent   Porfyri, akut intermittent
Location corresponding to Mesh Number C18.452.648.708.400.150

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Acute Intermittent   Porfyri, akut intermittent
Location corresponding to Mesh Number C18.452.811.400.150

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Acute Intermittent   Porfyri, akut intermittent
Location corresponding to Mesh Number C18.452.880.617.400.150

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Acute Intermittent   Porfyri, akut intermittent
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