hereditary spastic paraplegia 6
hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has material basis in mutation in the NIPA1 gene on chromosome 15q11.2
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Summary
hereditary spastic paraplegia 6 is a rare disease[1]. It is known by 10 alternative names across languages and contexts.[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: hereditary spastic paraplegia[4], pure or complex autosomal dominant spastic paraplegia[5], autosomal dominant disease[6]
- Health specialty: neurology[7]
- Genetic association: NIPA1[8]
- Exact match: http://purl.obolibrary.org/obo/DOID_0110811[9], http://identifiers.org/doid/DOID:0110811[10], http://www.orpha.net/ORDO/Orphanet_100988[11]
- On focus list of Wikimedia project: WikiProject Medicine[12]