Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandBasal Ganglia Diseases (D001480)
Parent Node:
expandCerebellar Ataxia (D002524)
..Starting node
..expandNeuhauser Eichner Opitz syndrome (C536407)

       Child Nodes:



 Sister Nodes: 
..expand3-Methylglutaconic Aciduria, Type V (C565706)
..expandAniridia cerebellar ataxia mental deficiency (C536370)
..expandAtaxia, Spastic, 1, Autosomal Dominant (C566993)
..expandAtaxia, Spastic, 2, Autosomal Recessive (C566969)
..expandAtaxia, Spastic, 3, Autosomal Recessive (C566956)
..expandAutosomal Recessive Cerebellar Ataxia Type 1 (C579934)
..expandBrachydactyly-Nystagmus-Cerebellar Ataxia (C566192)
..expandBranchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia (C566188)
..expandCAPOS syndrome (C535351)
..expandCerebellar Ataxia and Hypergonadotropic Hypogonadism (C565308)
..expandCerebellar Ataxia and Hypogonadotropic Hypogonadism (C565870)
..expandCerebellar Ataxia and Neurosensory Deafness (C565869)
..expandCerebellar ataxia ectodermal dysplasia (C535350)
..expandCerebellar Ataxia, Benign, with Thermoanalgesia (C565868)
..expandCerebellar Ataxia, Cayman Type (C563363)
..expandCerebellar Ataxia, Deafness, and Narcolepsy (C565825)
..expandCerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 (C567656)
..expandCerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 (C567690)
..expandCerebellar hypoplasia with endosteal sclerosis (C535353)
..expandCerebelloparenchymal Disorder II (C565866)
..expandDementia, familial Danish (C538209)
..expandDysequilibrium syndrome (C535731)
..expandEpisodic Ataxia, Type 5 (C566601)
..expandEpisodic Ataxia, Type 6 (C567207)
..expandFurukawa Takagi Nakao syndrome (C538193)
..expandHarding ataxia (C535633)
..expandHemiplegic migraine, familial type 1 (C536890)
..expandHerrmann syndrome (C538113)
..expandLaryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy (C565252)
..expandMainzer-Saldino Disease (C535463)
..expandMarinesco-Sjogren-like syndrome (MSLS) (C535913)
..expandMyelocerebellar Disorder (C563233)
..expandMyoclonus, Cerebellar Ataxia, and Deafness (C563549)
..expandNeuhauser Eichner Opitz syndrome (C536407)
..expandRenal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA (C564014)
..expandSpinocerebellar Ataxias (D020754) Child34
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:7915
Name:Neuhauser Eichner Opitz syndrome
Definition:
Alternative IDs:
ParentIDs:MESH:D001480|MESH:D002524
TreeNumbers:C10.228.140.079/C536407 |C10.228.140.252.190/C536407 |C10.597.350.090.500/C536407 |C23.888.592.350.090.200/C536407
Synonyms:Encephalopathy, recurrent, of childhood
Slim Mappings:Nervous system disease|Signs and symptoms
Reference: MedGen: C536407
MeSH: C536407
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants