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Metadata
ID DOID:0110772
Name hereditary spastic paraplegia 19
Definition A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 9q.
https://www.ncbi.nlm.nih.gov/pubmed/12112072
Xrefs

GARD:9588

ICD10CM:G11.4

OMIM:607152

ORDO:100999

Subsets

DO_rare_slim

Synonyms

autosomal dominant spastic paraplegia 19 [EXACT]

autosomal dominant spastic paraplegia type 19 [EXACT]

SPG19 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal dominant disease

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