Visualize Submit Comment
Metadata
ID DOID:0110786
Name hereditary spastic paraplegia 35
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1.
https://www.ncbi.nlm.nih.gov/pubmed/19068277
Xrefs

ICD10CM:G11.4

OMIM:612319

ORDO:171629

Synonyms

autosomal recessive spastic paraplegia 35 [EXACT]

autosomal recessive spastic paraplegia type 35 [EXACT]

FAHN [EXACT]

fatty acid hydroxylase-associated neurodegeneration [EXACT]

leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia [EXACT]

SPG35 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

Add an item to the term tracker