hereditary spastic paraplegia 62
hereditary spastic paraplegia that has material basis in mutation in the ERLIN1 gene on chromosome 10q24
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Summary
hereditary spastic paraplegia 62 is a rare disease[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- hereditary spastic paraplegia 62's instance of is recorded as rare disease[3].
- hereditary spastic paraplegia 62's instance of is recorded as class of disease[4].
- hereditary spastic paraplegia 62 is a type of hereditary spastic paraplegia[5].
- hereditary spastic paraplegia 62 is a type of autosomal recessive pure spastic paraplegia[6].
- hereditary spastic paraplegia 62 is a type of genetic disease[7].
- hereditary spastic paraplegia 62 is a type of autosomal recessive disease[8].
- hereditary spastic paraplegia 62's health specialty is recorded as neurology[9].
- hereditary spastic paraplegia 62's genetic association is recorded as ERLIN1[10].
- hereditary spastic paraplegia 62's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110813[11].
- hereditary spastic paraplegia 62's exact match is recorded as http://identifiers.org/doid/DOID:0110813[12].
- hereditary spastic paraplegia 62's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_401785[13].
- hereditary spastic paraplegia 62's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
hereditary spastic paraplegia 62 is known by 6 alternative names across languages and contexts.[2]