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- Q424247 subject Q6853345.
- Q424247 subject Q6949571.
- Q424247 abstract "Acute intermittent porphyria (AIP) is a rare autosomal dominant metabolic disorder affecting the production of heme, the oxygen-binding prosthetic group of hemoglobin. It is characterized by a deficiency of the enzyme porphobilinogen deaminase. Acute intermittent porphyria is the second most common form of porphyria (porphyria cutanea tarda being the most common). Its incidence is estimated to be between 5 and 10 in 100,000, but this is likely underestimated because of positive cases not being induced, and long periods of latency, with an estimation that it is latent in 90% of cases.".
- Q424247 icd10 "E80.2".
- Q424247 icd9 "277.1".
- Q424247 meshId "D017118".
- Q424247 omim "176000".
- Q424247 thumbnail Porphobilinogen.png?width=300.
- Q424247 wikiPageExternalLink 9159524.
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- Q424247 icd "277.1".
- Q424247 icd "E80.2".
- Q424247 meshid "D017118".
- Q424247 omim "176000".
- Q424247 type Disease.
- Q424247 type Thing.
- Q424247 type Q12136.
- Q424247 comment "Acute intermittent porphyria (AIP) is a rare autosomal dominant metabolic disorder affecting the production of heme, the oxygen-binding prosthetic group of hemoglobin. It is characterized by a deficiency of the enzyme porphobilinogen deaminase. Acute intermittent porphyria is the second most common form of porphyria (porphyria cutanea tarda being the most common).".
- Q424247 label "Acute intermittent porphyria".
- Q424247 depiction Porphobilinogen.png.