Search Ontology:

Human Disease

hereditary spastic paraplegia 19

Term ID

DOID:0110772

Synonyms

autosomal dominant spastic paraplegia 19
autosomal dominant spastic paraplegia type 19
SPG19

Definition

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 9q. https://www.ncbi.nlm.nih.gov/pubmed/12112072

References

GARD:9588
ICD10CM:G11.4
OMIM:607152
ORDO:100999

Ontology

Human Disease ( DOID:0110772 )

Relationships

is a type of: autosomal dominant disease hereditary spastic paraplegia

autosomal dominant disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models

Citations