ZFIN Human Disease: hereditary spastic paraplegia 24

OBO ID: DOID:0110775

OBO ID: DOID:0110775

Term Name:	hereditary spastic paraplegia 24	Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 24 autosomal recessive spastic paraplegia type 24 SPG24
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 13q14. https://www.ncbi.nlm.nih.gov/pubmed/12499481
References:	GARD:9296 ICD10CM:G11.4 OMIM:607584 ORDO:101004
Ontology:	Human Disease ( DOID:0110775 )

Relationships

is a type of:	autosomal recessive disease hereditary spastic paraplegia autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

OTHER hereditary spastic paraplegia 24 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None