| children | - Adult-onset autosomal recessive cerebellar ataxia 785302009
- Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula 1259123006
- Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea 1259121008
- ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis 789657008
- Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency 1237625002
- Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency 773498006
- Autosomal recessive cerebellar ataxia, psychomotor delay syndrome 783060009
- Birnbaum's syndrome 45814002
- Boucher Neuhäuser syndrome 715984007
- Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome 1236804009
- Cerebellar ataxia with oculomotor apraxia type 4 1217230002
- Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia 785301002
- Childhood-onset basal ganglia degeneration syndrome 1172584005
- Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder 1167373005
- Chronic bilirubin encephalopathy 1197758001
- Chronic brain-hydrocephalus syndrome 15139001
- Chronic cerebrovascular accident 434141000124103
- Chronic cluster headache 230473009
- Chronic hypoxic-ischemic brain injury 429271000124103
- Chronic intractable migraine without aura 124171000119105
- Chronic migraine without aura, non-refractory 437931000124100
- Chronic non-psychotic brain syndrome 27195007
- Chronic organic mental disorder 425919003
- Chronic progressive epilepsia partialis continua 39745004
- Chronic progressive non-hereditary chorea 3456001
- Chronic viral encephalitis 230179001
- Chronic viral hepatitis C with hepatic coma 435101000124104
- Congenital muscular dystrophy with cerebellar involvement 783176002
- Congenital muscular dystrophy with intellectual disability 783174004
- Congenital muscular dystrophy with intellectual disability and severe epilepsy 782772000
- Corticobasal syndrome 1230018005
- Cranio-cervical dystonia with laryngeal and upper limb involvement 783179009
- Dystonia 28 1281844004
- Early-onset calcifying leukoencephalopathy, skeletal dysplasia 1222661007
- Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome 1169356004
- Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome 1172588008
- Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome 771469002
- Endosteal hyperostoses with cerebellar hypoplasia 254132000
- Familial infantile bilateral striatal necrosis 1208478005
- Fatal post-viral neurodegenerative disorder 774206008
- Friedreich ataxia 10394003
- Gemignani syndrome 782690007
- Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome 1172696009
- Hereditary cerebral amyloid angiopathy, Icelandic type 45639009
- Huntington disease-like 3 770939009
- Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome 721846006
- Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly 770725000
- Infantile osteopetrosis with neuroaxonal dysplasia syndrome 724226009
- Intermittently raised pressure hydrocephalus 230748005
- ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement 1208747005
- MEPAN syndrome 1236805005
- Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007
- Multiple mitochondrial dysfunctions syndrome type 6 1279891002
- Muscle eye brain disease with bilateral multicystic leukodystrophy 785298001
- Myoclonic epilepsy with ragged red fibers 230426003
- Non-Alzheimer's progressive dysphasia 230279005
- Odontoleukodystrophy 722064003
- Parkinsonian syndrome with idiopathic orthostatic hypotension 72585000
- Paroxysmal choreoathetosis 49949003
- Paroxysmal dystonia 230310003
- Persistent vegetative state 24473007
- PLAA-associated neurodevelopmental disorder 1217367007
- Pontine autosomal dominant microangiopathy with leukoencephalopathy 1173997008
- Postpartum amenorrhea-galactorrhea syndrome 85039006
- Progressive aphasia 230278002
- Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome 1237413006
- Progressive cerebellar ataxia with hypogonadism 230240004
- Progressive cerebello-cerebral atrophy 1208481000
- Progressive congenital rubella encephalomyelitis 302811004
- Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009
- Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome 770678005
- Progressive external ophthalmoplegia, myopathy, emaciation syndrome 764733009
- Progressive focal cortical atrophy 737228009
- Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome 1172900005
- Progressive myoclonic epilepsy type 3 783064000
- Progressive myoclonic epilepsy type 5 783055005
- Progressive myoclonic epilepsy type 6 783062001
- Progressive myoclonic epilepsy type 7 1208939001
- Progressive myoclonic epilepsy type 8 783139000
- Progressive myoclonic epilepsy type 9 1228857005
- Progressive polyneuropathy with bilateral striatal necrosis 771305006
- Progressive post hemorrhagic ventricular dilatation 359629000
- Progressive supranuclear palsy 192976002
- PYCR2-related microcephaly, progressive leukoencephalopathy 1237421000
- Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations 783787000
- Rett syndrome 68618008
- Severe oculo-renal-cerebellar syndrome 1208341008
- Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006
- Spinocerebellar ataxia type 41 1208512000
- Spinocerebellar ataxia type 42 1208513005
- Spinocerebellar ataxia type 43 1208516002
- Spinocerebellar ataxia type 45 1279840000
- Spinocerebellar ataxia type 46 1279839002
- Van Bogaert's sclerosing leukoencephalitis 359686005
- Walker-Warburg congenital muscular dystrophy 111504002
- X-linked progressive cerebellar ataxia 827172005
|
Quick, Current, Complete - www.findacode.com