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Ontology Browser

Term:
childhood spinal muscular atrophy (DOID:0060160)
Annotations: Rat: (7) Mouse: (7) Human: (9) Chinchilla: (5) Bonobo: (5) Dog: (6) Squirrel: (5) Pig: (6)
Parent Terms Term With Siblings Child Terms
adult spinal muscular atrophy  
Alexander Disease  
anterior horn cell disease 
autosomal dominant adult-onset proximal spinal muscular atrophy  
autosomal dominant distal hereditary motor neuronopathy +   
autosomal recessive distal hereditary motor neuronopathy +   
Camptocormia  
Canavan disease  
Cerebrocortical Degeneration of Infancy 
childhood spinal muscular atrophy +   
A spinal muscular atrophy that is associated with the survival of motor neuron protein in childhood. (DO)
Cockayne syndrome +   
Congenital Muscular Dystrophy with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers 
Distal Hereditary Motor Neuropathy, Type II 
Dystonia Musculorum Deformans +   
Familial Amyloid Polyneuropathies +   
familial encephalopathy with neuroserpin inclusion bodies  
Gerstmann-Straussler-Scheinker syndrome  
Gilles de la Tourette syndrome +   
Hereditary Central Nervous System Demyelinating Diseases +   
Hereditary Optic Atrophies +   
hereditary sensory neuropathy +   
Huntington's disease +   
Huntington's disease-like 2  
Huntington's Disease-Like Syndrome  
Kennedy's disease  
Lafora disease  
Leukoencephalomyelopathy  
Lipodystrophy with Congenital Cataracts and Neurodegeneration  
Mental Retardation, X-Linked +   
mitochondrial DNA depletion syndrome 6  
motor peripheral neuropathy +   
myotonia congenita +   
myotonic dystrophy type 1 +   
neuroacanthocytosis +   
neurofibromatosis +   
neurogenic scapuloperoneal syndrome Kaeser type  
neuronal ceroid lipofuscinosis +   
Opticocochleodentate Degeneration 
pantothenate kinase-associated neurodegeneration +   
PCWH syndrome  
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain 
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
primary cerebellar degeneration +   
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
Progressive Psychomotor Deterioration  
scapuloperoneal spinal muscular atrophy  
spinal muscular atrophy with lower extremity predominance +   
Spinal Muscular Atrophy with Mental Retardation 
Spinal Muscular Atrophy, Facioscapulohumeral Type  
Spinal Muscular Atrophy, Jokela Type  
Spinal Muscular Atrophy, Ryukyuan Type 
Spinal Muscular Atrophy, Segmental 
Spongiform Encephalopathy with Neuropsychiatric Features  
syndromic microphthalmia 10 
tuberous sclerosis +   
Unverricht-Lundborg syndrome +   
Wilson disease +   
X-linked distal spinal muscular atrophy 3  
X-linked spinal muscular atrophy 2  

Synonyms
Exact Synonyms: Spinal Muscular Atrophy 1 ;   Spinal Muscular Atrophy, Mild Childhood and Adolescent Form ;   juvenile muscular atrophy ;   juvenile spinal muscular atrophy ;   spinal muscular atrophies of childhood ;   spinal muscular atrophy of childhood ;   survival motor neuron spinal muscular atrophy
Primary IDs: MESH:D014897
Xrefs: NCI:C85076 ;   ORDO:70
Definition Sources: url:http://en.wikipedia.org/wiki/Survival_motor_neuron_spinal_muscular_atrophy "DO"

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