SPOAN syndrome
gene (11q13.1), encoding kinesin light chain 2.
Press Enter · cited answer in seconds
0 sources
SPOAN syndrome
Summary
SPOAN syndrome is a rare disease[1]. It draws 44 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]
Key Facts
- SPOAN syndrome is credited with the discovery of Silvana Santos[3].
- SPOAN syndrome's instance of is recorded as rare disease[4].
- SPOAN syndrome's instance of is recorded as class of disease[5].
- SPOAN syndrome is a type of neurodegeneration[6].
- SPOAN syndrome is a type of spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder[7].
- SPOAN syndrome is a type of genetic disease[8].
- SPOAN syndrome is a type of autosomal recessive disease[9].
- SPOAN syndrome is a type of disease[10].
- SPOAN syndrome's health specialty is recorded as neurology[11].
- SPOAN syndrome's genetic association is recorded as KLC2[12].
- SPOAN syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060491[13].
- SPOAN syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060491[14].
- SPOAN syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_320406[15].
- SPOAN syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- SPOAN syndrome's on focus list of Wikimedia project is recorded as Q132578991[17].
Body
Works and Contributions
SPOAN syndrome is credited with the discovery of Silvana Santos[3].
Why It Matters
SPOAN syndrome draws 44 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2] It is known by 10 alternative names across languages and contexts.[18]