Disease Browser
Parent Node: frontotemporal degeneration with dementia (MONDO:0020137) Parent Node: frontotemporal neurodegeneration with movement disorder (MONDO:0017643) Parent Node: genetic neurodegenerative disease with dementia (MONDO:0021037) Parent Node: inherited tremor disorder (MONDO:0017663) ..Starting node .. corticobasal syndrome () Child Nodes:
Sister Nodes: ..arthrogryposis () ..ataxia with fasciculations () ..ataxia-hypogonadism-choroidal dystrophy syndrome () ..autosomal dominant cerebellar ataxia () ..autosomal dominant sensory ataxia 1 () ..autosomal recessive cerebellar ataxia () ..autosomal recessive limb-girdle muscular dystrophy type 2S () ..behavioral variant of frontotemporal dementia () ..bilateral striopallidodentate calcinosis () ..cataract-ataxia-deafness syndrome () ..cerebellar ataxia-hypogonadism syndrome () ..childhood-onset benign chorea with striatal involvement () ..chorea () ..chorea, remitting, with nystagmus and cataract () ..choreoathetosis, familial inverted () ..corticobasal syndrome () ..episodic ataxia type 1 () ..ETM2 () ..ETM3 () ..familial infantile bilateral striatal necrosis () L: 00075 ; ..frontotemporal dementia with motor neuron disease () ..hereditary geniospasm () ..hereditary hyperekplexia () ..hereditary spastic paraplegia 7 () L: 00497 ; ..Huntington disease () ..Huntington disease-like 1 () ..Huntington disease-like 3 () ..Huntington disease-like syndrome due to C9ORF72 expansions () ..ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome () ..inherited Creutzfeldt-Jakob disease () ..inherited dystonia () ..juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome () ..mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome () L: 00532 ; ..monogenic disease with epilepsy () ..muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome () ..myoclonus-cerebellar ataxia-deafness syndrome () ..neuroacanthocytosis () ..neurodegeneration with brain iron accumulation () ..neuronal intranuclear inclusion disease () ..primary myoclonus () ..progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome () ..progressive non-fluent aphasia () ..progressive supranuclear palsy () ..rare genetic disease with myoclonus as a major feature () ..Richards-Rundle syndrome () ..sensorineural hearing loss-early graying-essential tremor syndrome () ..spasticity-ataxia-gait anomalies syndrome () ..Tourette syndrome () ..tremor, hereditary essential, 1 () ..tremor, hereditary essential, 4 () ..tremor, hereditary essential, 5 () ..Williams syndrome () ..X-linked cerebellar ataxia () MONDO is developed by the Monarch Initiative . Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM ,ClinVar , CTD