Alström syndrome
rare genetic disorder caused by mutations in the gene ALMS1
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Alström syndrome
Summary
Alström syndrome is a genetic disease[1]. It draws 38 Wikipedia views per month (genetic_disease category, ranking #3 of 16).[2]
Key Facts
- Alström syndrome's instance of is recorded as genetic disease[3].
- Alström syndrome's instance of is recorded as rare disease[4].
- Alström syndrome's instance of is recorded as class of disease[5].
- Carl-Henry Alström is named after Alström syndrome[6].
- Alström syndrome is a type of hereditary motor and sensory neuropathy[7].
- Alström syndrome is a type of autosomal recessive disease[8].
- Alström syndrome is a type of syndrome[9].
- Alström syndrome is a type of disease[10].
- Alström syndrome's Commons category is recorded as Alström syndrome[11].
- Alström syndrome's symptoms and signs is recorded as blindness[12].
- Alström syndrome's NCI Thesaurus ID is recorded as C84549[13].
- Alström syndrome's health specialty is recorded as medical genetics[14].
- Alström syndrome's health specialty is recorded as ophthalmology[15].
- Alström syndrome's health specialty is recorded as neurology[16].
- Alström syndrome's genetic association is recorded as ALMS1[17].
- Alström syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050473[18].
- Alström syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050473[19].
- Alström syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
Why It Matters
Alström syndrome draws 38 Wikipedia views per month (genetic_disease category, ranking #3 of 16).[2] It has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[21] It is known by 12 alternative names across languages and contexts.[22]