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Metadata
ID DOID:0110774
Name hereditary spastic paraplegia 23
Definition A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32.
https://www.ncbi.nlm.nih.gov/pubmed/14681889
Xrefs

GARD:336

ICD10CM:G11.4

OMIM:270750

ORDO:101003

Subsets

DO_rare_slim

Synonyms

Lison syndrome [EXACT]

Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome [EXACT]

spastic paraplegia 23 [EXACT]

spastic paraplegia with pigmentary abnormalities [EXACT]

SPG23 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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