hereditary spastic paraplegia 26
gene (12q13.3), encoding Beta-1, 4 N-acetylgalactosaminyltransferase 1.
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Summary
hereditary spastic paraplegia 26 is a rare disease[1]. It is known by 8 alternative names across languages and contexts.[2]
Key Facts
- hereditary spastic paraplegia 26's instance of is recorded as rare disease[3].
- hereditary spastic paraplegia 26's instance of is recorded as class of disease[4].
- hereditary spastic paraplegia 26 is a type of hereditary spastic paraplegia[5].
- hereditary spastic paraplegia 26 is a type of autosomal recessive complex spastic paraplegia[6].
- hereditary spastic paraplegia 26 is a type of autosomal recessive disease[7].
- hereditary spastic paraplegia 26's health specialty is recorded as neurology[8].
- hereditary spastic paraplegia 26's genetic association is recorded as B4GALNT1[9].
- hereditary spastic paraplegia 26's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110777[10].
- hereditary spastic paraplegia 26's exact match is recorded as http://identifiers.org/doid/DOID:0110777[11].
- hereditary spastic paraplegia 26's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101006[12].
- hereditary spastic paraplegia 26's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
hereditary spastic paraplegia 26 is known by 8 alternative names across languages and contexts.[2]