ZFIN Human Disease: hereditary spastic paraplegia 14

OBO ID: DOID:0110767

OBO ID: DOID:0110767

Term Name:	hereditary spastic paraplegia 14	Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 14 autosomal recessive spastic paraplegia type 14 SPG14
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 3q27-q28. https://www.ncbi.nlm.nih.gov/pubmed/10877981
References:	GARD:9589 ICD10CM:G11.4 OMIM:605229 ORDO:100995
Ontology:	Human Disease ( DOID:0110767 )

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 14 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None