ONTOLOGY REPORT - ANNOTATIONS


Term:cerebral palsy
go back to main search page
Accession:DOID:1969 term browser browse the term
Definition:A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)
Synonyms:exact_synonym: CP (cerebral palsy);   Dystonic-Rigid Cerebral Palsies;   Dystonic-Rigid Cerebral Palsy;   Hypotonic Cerebral Palsies;   Hypotonic Cerebral Palsy;   Monoplegic Cerebral Palsies;   Rolandic type cerebral palsy;   athetoid cerebral palsies;   athetoid cerebral palsy;   atonic cerebral palsy;   congenital cerebral palsy;   infantile cerebral palsy;   monoplegic cerebral palsy;   monoplegic infantile cerebral palsy
 primary_id: MESH:D002547
 alt_id: RDO:0001598
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
cerebral palsy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Add3 adducin 3 JBrowse link 1 273,854,195 273,961,982 RGD:8554872
G Aif1 allograft inflammatory factor 1 JBrowse link 20 5,161,350 5,167,176 RGD:2313028
G Alox5ap arachidonate 5-lipoxygenase activating protein JBrowse link 12 6,854,930 6,879,112 RGD:2313892
G Pomc proopiomelanocortin JBrowse link 6 28,382,937 28,388,771 RGD:11554173
hereditary spastic paraplegia 50 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Add3 adducin 3 JBrowse link 1 273,854,195 273,961,982 RGD:8554872
RGD:7240710
G Ap4m1 adaptor related protein complex 4 subunit mu 1 JBrowse link 12 19,314,222 19,320,339 RGD:7240710
RGD:8554872
G Mcm7 minichromosome maintenance complex component 7 JBrowse link 12 19,306,615 19,313,877 RGD:8554872
NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Wdr45b WD repeat domain 45B JBrowse link 10 110,523,843 110,555,769 RGD:8554872
RGD:7240710
Renpenning syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Pqbp1 polyglutamine binding protein 1 JBrowse link X 15,448,570 15,453,130 RGD:7240710
RGD:8554872
RGD:11554173
Spastic Cerebral Palsy, Quadriplegic, 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gad1 glutamate decarboxylase 1 JBrowse link 3 56,861,440 56,902,139 RGD:7240710
RGD:8554872
Spastic Cerebral Palsy, Quadriplegic, 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kank1 KN motif and ankyrin repeat domains 1 JBrowse link 1 243,201,073 243,398,531 RGD:7240710
RGD:8554872
spastic diplegia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Spast spastin JBrowse link 6 22,230,067 22,282,166 RGD:8554872
spastic quadriplegia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gad1 glutamate decarboxylase 1 JBrowse link 3 56,861,440 56,902,139 RGD:13592920
RGD:8554872
G Kank1 KN motif and ankyrin repeat domains 1 JBrowse link 1 243,201,073 243,398,531 RGD:13592920

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        central nervous system disease 6908
          brain disease 6412
            Chronic Brain Damage 13
              cerebral palsy 11
                Dysmyelination with Jaundice 0
                Neuhauser Syndrome 0
                Paine Syndrome 0
                Renpenning syndrome 1
                ataxic cerebral palsy 0
                dyskinetic cerebral palsy 0
                hereditary spastic paraplegia 50 3
                mixed cerebral palsy 0
                spastic cerebral palsy + 4
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.