ZFIN Human Disease: hereditary spastic paraplegia 26

OBO ID: DOID:0110777

Term Name:	hereditary spastic paraplegia 26		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 26 autosomal recessive spastic paraplegia type 26 GM2 synthase deficiency SPG26
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the B4GALNT1 gene on chromosome 12q13. https://www.ncbi.nlm.nih.gov/pubmed/23746551
References:	GARD:9587 ICD10CM:G11.4 OMIM:609195 ORDO:101006
Ontology:	Human Disease ( DOID:0110777 )

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 26 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
B4GALNT1	b4galnt1a b4galnt1b	Spastic paraplegia 26, autosomal recessive	609195

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None