hereditary spastic paraplegia 3A
hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has material basis in mutation in the ATL1 gene on chromosome 14q22
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hereditary spastic paraplegia 3A
Summary
hereditary spastic paraplegia 3A is a rare disease[1]. It is known by 14 alternative names across languages and contexts.[2]
Key Facts
- hereditary spastic paraplegia 3A's instance of is recorded as rare disease[3].
- hereditary spastic paraplegia 3A's instance of is recorded as class of disease[4].
- hereditary spastic paraplegia 3A is a type of hereditary spastic paraplegia[5].
- hereditary spastic paraplegia 3A is a type of pure or complex autosomal dominant spastic paraplegia[6].
- hereditary spastic paraplegia 3A is a type of autosomal dominant disease[7].
- hereditary spastic paraplegia 3A's NCI Thesaurus ID is recorded as C142893[8].
- hereditary spastic paraplegia 3A's health specialty is recorded as neurology[9].
- hereditary spastic paraplegia 3A's genetic association is recorded as ATL1[10].
- hereditary spastic paraplegia 3A's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110791[11].
- hereditary spastic paraplegia 3A's exact match is recorded as http://identifiers.org/doid/DOID:0110791[12].
- hereditary spastic paraplegia 3A's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_100984[13].
- hereditary spastic paraplegia 3A's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
hereditary spastic paraplegia 3A is known by 14 alternative names across languages and contexts.[2]