|  Help  |  About  |  Contact Us

DO Term : hereditary spastic paraplegia 11 [DOID:0110764] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21.
  • synonyms:
  • autosomal recessive spastic paraplegia complicated with thin corpus callosum,
  • OMIM:604360,
  • autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum,
  • HSP-TCC,
  • GARD:4919,
  • SPG11,
  • 604360,
  • ORDO:2822,
  • autosomal recessive spastic paraplegia type 11,
  • ICD10CM:G11.4,
  • Nakamura-Osame syndrome,
  • spastic paraplegia-intellectual disability-thin corpus callosum syndrome,
  • autosomal recessive spastic paraplegia 11
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents