hereditary spastic paraplegia 50
hereditary spastic paraplegia that has material basis in mutation in the AP4M1 gene on chromosome 7q22.1
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Summary
hereditary spastic paraplegia 50 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], severe intellectual disability and progressive spastic paraplegia[5], autosomal recessive disease[6]
- NCI Thesaurus ID: C179863[7]
- Genetic association: AP4M1[8]
- Exact match: http://purl.obolibrary.org/obo/DOID_0110802[9], http://identifiers.org/doid/DOID:0110802[10], http://www.orpha.net/ORDO/Orphanet_280763[11]
- On focus list of Wikimedia project: WikiProject Medicine[12]