bn:02028114n
Noun Concept
Categories: Skin conditions resulting from errors in metabolism, Porphyrias, Autosomal recessive disorders
EN
aminolevulinic acid dehydratase deficiency porphyria  Porphyria due to ALAD deficiency  acute porphyria  ALA-D deficiency porphyria  ALA deficiency porphyria
EN
Aminolevulinic acid dehydratase deficiency porphyria is an extremely rare autosomal recessive metabolic disorder that results from inappropriately low levels of the enzyme delta-aminolevulinic acid dehydratase, which is required for normal heme synthesis. Wikipedia
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EN
Aminolevulinic acid dehydratase deficiency porphyria is an extremely rare autosomal recessive metabolic disorder that results from inappropriately low levels of the enzyme delta-aminolevulinic acid dehydratase, which is required for normal heme synthesis. Wikipedia
Porphyria that has symptom abdominal pain, has symptom neuropathy, has symptom autonomic instability and has symptom psychosis Wikidata