hereditary spastic paraplegia 15
hereditary spastic paraplegia that has material basis in mutation in the ZFYVE26 gene on chromosome 14q24.1
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Summary
hereditary spastic paraplegia 15 is a rare disease[1]. It draws 72 Wikipedia views per month (rare disease category, ranking #236 of 627).[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: hereditary spastic paraplegia[4], autosomal recessive complex spastic paraplegia[5], autosomal recessive disease[6]
- Prevalence: 0.000001[7]
- Health specialty: neurology[8]
- Genetic association: ZFYVE26[9]
- Age of onset: juvenile onset[10], adult onset[11], childhood onset[12]
- Exact match: http://purl.obolibrary.org/obo/DOID_0110768[13], http://identifiers.org/doid/DOID:0110768[14], http://www.orpha.net/ORDO/Orphanet_100996[15]
- On focus list of Wikimedia project: WikiProject Medicine[16]
- Has phenotype: spasticity[17], gait abnormality[18], muscle weakness[19], basal ganglia disease[20], Q141815173[21], leukoaraiosis[22], Babinski sign[23], pseudobulbar palsy[24], demyelinating polyneuropathy[25], Q141816369[26], pathologic nystagmus[27], behavioral abnormality[28], dementia[29], diabetes[30]
- P14914: D100996[31]
Why It Matters
hereditary spastic paraplegia 15 is known by 11 alternative names across languages and contexts.[32]