hereditary spastic paraplegia 77
hereditary spastic paraplegia that has material basis in mutation in the FARS2 gene on chromosome 6p25
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Summary
hereditary spastic paraplegia 77 is a developmental defect during embryogenesis[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- hereditary spastic paraplegia 77's instance of is recorded as developmental defect during embryogenesis[3].
- hereditary spastic paraplegia 77's instance of is recorded as rare disease[4].
- hereditary spastic paraplegia 77's instance of is recorded as class of disease[5].
- hereditary spastic paraplegia 77 is a type of hereditary spastic paraplegia[6].
- hereditary spastic paraplegia 77 is a type of nervous system heredodegenerative disease[7].
- hereditary spastic paraplegia 77 is a type of rare genetic developmental defect during embryogenesis[8].
- hereditary spastic paraplegia 77 is a type of combined oxidative phosphorylation deficiency[9].
- hereditary spastic paraplegia 77 is a type of autosomal recessive disease[10].
- hereditary spastic paraplegia 77's health specialty is recorded as neurology[11].
- hereditary spastic paraplegia 77's genetic association is recorded as FARS2[12].
- hereditary spastic paraplegia 77's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110822[13].
- hereditary spastic paraplegia 77's exact match is recorded as http://identifiers.org/doid/DOID:0110822[14].
- hereditary spastic paraplegia 77's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_466722[15].
- hereditary spastic paraplegia 77's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
hereditary spastic paraplegia 77 is known by 6 alternative names across languages and contexts.[2]