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ataxic cerebral palsy (DOID:0050670)
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Parent Terms Term With Siblings Child Terms
Ataxia +     
cerebral palsy +     
genetic disease +     
Abetalipoproteinemia Neuropathy  
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
adult-onset ataxia and polyneuropathy  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Alagille syndrome  
Alpha-2-Deficient Collagen Disease 
apparent mineralocorticoid excess syndrome  
Aquaporin 1 Deficiency 
Arts syndrome  
Ataxia with Fasciculations 
Ataxia with Myoclonic Epilepsy and Presenile Dementia 
Ataxia, Deafness, and Cardiomyopathy 
Ataxia-Microcephaly-Cataract Syndrome 
Ataxia-Oculomotor Apraxia 4  
ataxic cerebral palsy 
A cerebral palsy that is caused by damage to the cerebellum, which affects muscle coordination, particularly in the limb. Some individuals suffer from hypotonia, tremors, difficulty with visual and/or auditory processing. (DO)
Atonic-Astatic Syndrome of Foerster 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune lymphoproliferative syndrome +   
Bangstad Syndrome 
Behr syndrome  
Benign Childhood Paroxysmal Tonic Upgaze with Ataxia 
Bhaskar Jagannathan Syndrome 
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
CANOMAD Syndrome 
Carnitine Acetyltransferase Deficiency  
cataract 23  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cataract Ataxia Deafness 
Cataracts, Ataxia, Short Stature, and Mental Retardation 
Cenani-Lenz syndactyly syndrome  
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
CHARGE syndrome  
Childhood-onset Neurodegeneration with Ataxia, Tremor, Optic Atrophy, and Cognitive Decline  
Christianson syndrome  
chromosomal disease +   
COACH syndrome  
coenzyme Q10 deficiency disease +   
complement factor I deficiency  
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
complex cortical dysplasia with other brain malformations 7  
congenital diarrhea +   
congenital hemolytic anemia +   
Congenital Hepatic Fibrosis  
congenital hypoplastic anemia +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
Congenital Pain Insensitivity +   
Deafness Hyperuricemia Neurologic Ataxia 
desquamative interstitial pneumonia  
Dwarfism +   
dyskinetic cerebral palsy 
Dysmyelination with Jaundice 
Erythrokeratodermia with Ataxia 
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
familial isolated deficiency of vitamin E  
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
frontotemporal dementia and/or amyotrophic lateral sclerosis-3  
frontotemporal dementia and/or amyotrophic lateral sclerosis-4  
Gait Ataxia +   
Genetic Skin Diseases +   
Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine  
hereditary angioedema +   
hereditary ataxia +   
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
hereditary spastic paraplegia 50  
hypogonadotropic hypogonadism 5 with or without anosmia +   
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
Hypotonia, Congenital Nystagmus, Ataxia and Abnormal Auditory Brainstem Response 
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Joubert syndrome 7  
Kallmann syndrome +   
Lennox-Gastaut syndrome  
Leukoencephalopathy with Ataxia  
Marfan syndrome +   
Mitochondrial Myopathy, and Ataxia  
mixed cerebral palsy 
monogenic disease +   
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
Myokymia 1  
Nervous System Heredodegenerative Disorders +   
Neuhauser Syndrome 
Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia, and Ataxia   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
optic atrophy 10  
osteochondrodysplasia +   
Paine Syndrome 
Partington syndrome  
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
PHARC syndrome  
polygenic disease +   
Posterior Column Ataxia with Retinitis Pigmentosa  
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
progressive myoclonus epilepsy 1B  
pulmonary alveolar microlithiasis  
Reardon Wilson Cavanagh Syndrome 
Renpenning syndrome  
Richards-Rundle Syndrome 
Sacral Agenesis with Vertebral Anomalies  
Sensory Ataxia, Autosomal Dominant  
Spastic Ataxia with Congenital Miosis 
spastic cerebral palsy +   
Spastic Paraplegia, Ataxia, and Mental Retardation 
Spinocerebellar Ataxias +   
spondyloepimetaphyseal dysplasia, Genevieve-type  
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
Tapetoretinal Degeneration with Ataxia 
Treft Sanborn Carey Syndrome 
Tremor of Intention, Ataxia, and Lipofuscinosis 
Tryptophanuria with Dwarfism 
yellow nail syndrome +  

Exact Synonyms: ACP ;   ataxic cerebral palsy, autosomal recessive ;   hypotonic cerebral palsy
Primary IDs: MESH:C562856
Alternate IDs: OMIM:605388 ;   RDO:0012394
Xrefs: GARD:10451
Definition Sources: "DO", "DO"

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