acute intermittent porphyria
human disease
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acute intermittent porphyria
Summary
acute intermittent porphyria is a rare disease[1]. It draws 1,379 Wikipedia views per month (rare_disease category, ranking #97 of 627).[2]
Key Facts
- acute intermittent porphyria's instance of is recorded as rare disease[3].
- acute intermittent porphyria's instance of is recorded as class of disease[4].
- acute intermittent porphyria is a type of porphyria due to ALAD deficiency[5].
- acute intermittent porphyria is a type of porphyria[6].
- acute intermittent porphyria is a type of disease[7].
- acute intermittent porphyria's mode of inheritance is recorded as autosomal dominant[8].
- acute intermittent porphyria's NCI Thesaurus ID is recorded as C84536[9].
- acute intermittent porphyria's health specialty is recorded as endocrinology[10].
- acute intermittent porphyria's drug or therapy used for treatment is recorded as chlorpromazine[11].
- acute intermittent porphyria's genetic association is recorded as HMBS[12].
- acute intermittent porphyria's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3890[13].
- acute intermittent porphyria's exact match is recorded as http://identifiers.org/doid/DOID:3890[14].
- acute intermittent porphyria's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
acute intermittent porphyria draws 1,379 Wikipedia views per month (rare_disease category, ranking #97 of 627).[2] It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[16] It is known by 8 alternative names across languages and contexts.[17]