hereditary spastic paraplegia 11
hereditary spastic paraplegia that has material basis in mutation in the SPG11 gene on chromosome 15q21
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Summary
hereditary spastic paraplegia 11 is a rare disease[1]. It is known by 14 alternative names across languages and contexts.[2]
Key Facts
- hereditary spastic paraplegia 11's instance of is recorded as rare disease[3].
- hereditary spastic paraplegia 11's instance of is recorded as class of disease[4].
- hereditary spastic paraplegia 11 is a type of hereditary spastic paraplegia[5].
- hereditary spastic paraplegia 11 is a type of pure or complex autosomal recessive spastic paraplegia[6].
- hereditary spastic paraplegia 11 is a type of complex hereditary spastic paraplegia[7].
- hereditary spastic paraplegia 11 is a type of genetic syndromic intellectual disability[8].
- hereditary spastic paraplegia 11 is a type of genetic disease[9].
- hereditary spastic paraplegia 11 is a type of autosomal recessive disease[10].
- hereditary spastic paraplegia 11's NCI Thesaurus ID is recorded as C148317[11].
- hereditary spastic paraplegia 11's health specialty is recorded as neurology[12].
- hereditary spastic paraplegia 11's genetic association is recorded as SPG11[13].
- hereditary spastic paraplegia 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110764[14].
- hereditary spastic paraplegia 11's exact match is recorded as http://identifiers.org/doid/DOID:0110764[15].
- hereditary spastic paraplegia 11's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2822[16].
- hereditary spastic paraplegia 11's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
hereditary spastic paraplegia 11 is known by 14 alternative names across languages and contexts.[2]