Disease Information for Porphyria, acute intermittent: Disease Mechanism & Classification

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Class
CLASS/Pediatric disorders (ex)
CLASS/Hematologic (category)
CLASS/Systemic/no comment (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hepatic porphyria
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Porphobilinogen diaminase deficiency
Pathophysiology/Thermoregulatory defect
Pathophysiology/Delayed gastric emptying/gastrostasis
Pathophysiology/Demyelination
Pathophysiology/Lung Ventilation Neuromuscular
Pathophysiology/Hereditary deafness
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Enzyme defect/Metabolic disorder (ex)
PROCESS/Ethnic predilection (ex)
PROCESS/Genetic expressivity variable (ex)
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Metabolic porphyrin disorder (ex)
PROCESS/Metabolic/storage disorder (category)
PROCESS/Hereditory motor/sensory neuropathy (ex)
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