hereditary spastic paraplegia 48
hereditary spastic paraplegia that has material basis in mutation in the AP5Z1 gene on chromosome 7p22.1
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Summary
hereditary spastic paraplegia 48 is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- hereditary spastic paraplegia 48's instance of is recorded as rare disease[3].
- hereditary spastic paraplegia 48's instance of is recorded as class of disease[4].
- hereditary spastic paraplegia 48 is a type of hereditary spastic paraplegia[5].
- hereditary spastic paraplegia 48 is a type of pure or complex autosomal recessive spastic paraplegia[6].
- hereditary spastic paraplegia 48 is a type of nervous system heredodegenerative disease[7].
- hereditary spastic paraplegia 48 is a type of neurometabolic disease[8].
- hereditary spastic paraplegia 48 is a type of autosomal recessive disease[9].
- hereditary spastic paraplegia 48's health specialty is recorded as neurology[10].
- hereditary spastic paraplegia 48's genetic association is recorded as AP5Z1[11].
- hereditary spastic paraplegia 48's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110800[12].
- hereditary spastic paraplegia 48's exact match is recorded as http://identifiers.org/doid/DOID:0110800[13].
- hereditary spastic paraplegia 48's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_306511[14].
- hereditary spastic paraplegia 48's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
hereditary spastic paraplegia 48 is known by 7 alternative names across languages and contexts.[2]