hereditary spastic paraplegia 72
hereditary spastic paraplegia that has material basis in mutation in the REEP2 gene on chromosome 5q31
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Summary
hereditary spastic paraplegia 72 is a rare disease[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: hereditary spastic paraplegia[4], pure hereditary spastic paraplegia[5], genetic disease[6], autosomal dominant disease[7], autosomal recessive disease[8]
- Health specialty: neurology[9]
- Genetic association: REEP2[10]
- Exact match: http://purl.obolibrary.org/obo/DOID_0110817[11], http://identifiers.org/doid/DOID:0110817[12], http://www.orpha.net/ORDO/Orphanet_401849[13]
- On focus list of Wikimedia project: WikiProject Medicine[14]