hereditary spastic paraplegia 56
hereditary spastic paraplegia that has material basis in mutation in the CYP2U1 gene on chromosome 4q25
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Summary
hereditary spastic paraplegia 56 is a rare disease[1]. It is known by 7 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 recessive spastic paraplegia[5], autosomal recessive disease[6]
- NCI Thesaurus ID: C190870[7]
- Health specialty: neurology[8]
- Genetic association: CYP2U1[9]
- Exact match: http://purl.obolibrary.org/obo/DOID_0110808[10], http://identifiers.org/doid/DOID:0110808[11], http://www.orpha.net/ORDO/Orphanet_320411[12]
- On focus list of Wikimedia project: WikiProject Medicine[13]