hereditary spastic paraplegia 35

Term ID

DOID:0110786

Synonyms

• autosomal recessive spastic paraplegia 35
• autosomal recessive spastic paraplegia type 35
• FAHN
• fatty acid hydroxylase-associated neurodegeneration
• leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
• SPG35

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

References

• ICD10CM:G11.4
• OMIM:612319
• ORDO:171629

Ontology

Human Disease   ( DOID:0110786 )