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Metadata
ID DOID:0110812
Name hereditary spastic paraplegia 61
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12.
https://www.ncbi.nlm.nih.gov/pubmed/24482476
Xrefs

ICD10CM:G11.4

OMIM:615685

ORDO:401780

Synonyms

autosomal recessive spastic paraplegia 61 [EXACT]

autosomal recessive spastic paraplegia type 61 [EXACT]

SPG61 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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