hereditary spastic paraplegia 12
hereditary spastic paraplegia that has material basis in mutation in the RTN2 gene on chromosome 19q13
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Summary
hereditary spastic paraplegia 12 is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- hereditary spastic paraplegia 12's instance of is recorded as rare disease[3].
- hereditary spastic paraplegia 12's instance of is recorded as class of disease[4].
- hereditary spastic paraplegia 12 is a type of hereditary spastic paraplegia[5].
- hereditary spastic paraplegia 12 is a type of autosomal dominant pure spastic paraplegia[6].
- hereditary spastic paraplegia 12 is a type of autosomal dominant disease[7].
- hereditary spastic paraplegia 12's health specialty is recorded as neurology[8].
- hereditary spastic paraplegia 12's genetic association is recorded as RTN2[9].
- hereditary spastic paraplegia 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110765[10].
- hereditary spastic paraplegia 12's exact match is recorded as http://identifiers.org/doid/DOID:0110765[11].
- hereditary spastic paraplegia 12's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_100993[12].
- hereditary spastic paraplegia 12's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
hereditary spastic paraplegia 12 is known by 7 alternative names across languages and contexts.[2]