ZFIN Human Disease: hereditary spastic paraplegia 11

OBO ID: DOID:0110764

Term Name:	hereditary spastic paraplegia 11		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 11 autosomal recessive spastic paraplegia complicated with thin corpus callosum autosomal recessive spastic paraplegia type 11 autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum HSP-TCC Nakamura-Osame syndrome spastic paraplegia-intellectual disability-thin corpus callosum syndrome SPG11
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/17322883
References:	GARD:4919 ICD10CM:G11.4 OMIM:604360 ORDO:2822
Ontology:	Human Disease ( DOID:0110764 )

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 11 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SPG11	spg11	Spastic paraplegia 11, autosomal recessive	604360

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS (1)