| Help | About | Contact Us

DO Term : hereditary spastic paraplegia [DOID:2476] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs.

synonyms:
Strumpell-Lorrain disease,
PS303350,
French settlement disease,
ICD10CM:G11.4,
UMLS_CUI:C0037773,
GARD:6637,
hereditary spastic paraparesis,
MESH:D015419,
familial spastic paraplegia,
ICD9CM:334.1,
SNOMEDCT_US_2023_03_01:267692008,
OMIM:PS303350,
NCI:C140267

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

Questions? Comments? Click here!

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.

Your name:
Your email address:
Subject:
Message:	---- Current page: ---- /mousemine/report.do?id=77328907&trail=%7C77328907

MouseMine