complex hereditary spastic paraplegia

Findings

No curated finding names complex hereditary spastic paraplegia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

Where it sits

A kind of

• hereditary spastic paraplegia
• syndromic disease

Narrower terms (50)

• autosomal dominant complex spastic paraplegia
• autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction
• autosomal recessive complex spastic paraplegia type 9B
• autosomal recessive spastic paraplegia type 59
• autosomal recessive spastic paraplegia type 60
• autosomal recessive spastic paraplegia type 66
• autosomal recessive spastic paraplegia type 67
• autosomal recessive spastic paraplegia type 68
• autosomal recessive spastic paraplegia type 69
• autosomal recessive spastic paraplegia type 70
• autosomal recessive spastic paraplegia type 76
• autosomal recessive spastic paraplegia type 78
• fatty acid hydroxylase-associated neurodegeneration
• glutamate pyruvate transaminase 2 deficiency
• hereditary sensory and autonomic neuropathy with spastic paraplegia

Resolves to: complex hereditary spastic paraplegia

Also called

Complex familial spastic paraplegiaComplex HSPComplex SPGcomplicated familial spastic paraplegiacomplicated hereditary spastic paraplegiacomplicated HSPcomplicated SPGsyndrome associated with hereditary spastic paraplegiasyndromic hereditary spastic paraplegia