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Metadata
ID DOID:0110822
Name hereditary spastic paraplegia 77
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the FARS2 gene on chromosome 6p25.
https://www.ncbi.nlm.nih.gov/pubmed/26553276
Xrefs

ICD10CM:G11.4

OMIM:617046

ORDO:466722

Synonyms

autosomal recessive spastic paraplegia 77 [EXACT]

SPG77 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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