Behr syndrome
medical condition
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Behr syndrome
Summary
Behr syndrome is a rare disease[1]. It draws 50 Wikipedia views per month (rare_disease category, ranking #231 of 627).[2]
Key Facts
- Behr syndrome's instance of is recorded as rare disease[3].
- Behr syndrome's instance of is recorded as class of disease[4].
- Behr syndrome is a type of syndromic hereditary optic neuropathy[5].
- Behr syndrome is a type of neurological disorder[6].
- Behr syndrome is a type of autosomal recessive disease[7].
- Behr syndrome's NCI Thesaurus ID is recorded as C177251[8].
- Behr syndrome's genetic association is recorded as OPA1[9].
- Behr syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1239[10].
- Behr syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111580[11].
- Behr syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111580[12].
- Behr syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
Behr syndrome draws 50 Wikipedia views per month (rare_disease category, ranking #231 of 627).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[14] It is known by 5 alternative names across languages and contexts.[15]