hereditary spastic paraplegia 52
hereditary spastic paraplegia that has material basis in mutation in the AP4S1 gene on chromosome 14q12
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Summary
hereditary spastic paraplegia 52 is a rare disease[1]. It is known by 10 alternative names across languages and contexts.[2]
Key Facts
- hereditary spastic paraplegia 52's instance of is recorded as rare disease[3].
- hereditary spastic paraplegia 52's instance of is recorded as class of disease[4].
- hereditary spastic paraplegia 52 is a type of hereditary spastic paraplegia[5].
- hereditary spastic paraplegia 52 is a type of severe intellectual disability and progressive spastic paraplegia[6].
- hereditary spastic paraplegia 52 is a type of autosomal recessive disease[7].
- hereditary spastic paraplegia 52's NCI Thesaurus ID is recorded as C212890[8].
- hereditary spastic paraplegia 52's genetic association is recorded as AP4S1[9].
- hereditary spastic paraplegia 52's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110804[10].
- hereditary spastic paraplegia 52's exact match is recorded as http://identifiers.org/doid/DOID:0110804[11].
- hereditary spastic paraplegia 52's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_280763[12].
- hereditary spastic paraplegia 52's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
hereditary spastic paraplegia 52 is known by 10 alternative names across languages and contexts.[2]