|  Help  |  About  |  Contact Us

DO Term : hereditary spastic paraplegia 4 [DOID:0110792] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has_material_basis_in mutation in the SPAST gene on chromosome 2p22.
  • synonyms:
  • autosomal dominant spastic paraplegia type 4,
  • SPG4,
  • ORDO:100985,
  • ICD10CM:G11.4,
  • 182601,
  • autosomal dominant spastic paraplegia 4,
  • OMIM:182601
Paste the following link
Quick Links:
SummaryDiseaseOntology
 
Quick Links:
SummaryDiseaseOntology
 
Lists
This DOTerm isn't in any lists. Upload a list.

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





MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

Copyright © 2017 by The Jackson Laboratory. All Rights Reserved

© 2002 - 2017 Department of Genetics, University of Cambridge, Downing Street,
Cambridge CB2 3EH, United Kingdom