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:
expandNarcolepsy (D009290)
..Starting node
..expandCataplexy (D002385)

       Child Nodes:



 Sister Nodes: 
..expandCataplexy (D002385)
..expandCerebellar Ataxia, Deafness, and Narcolepsy (C565825)
..expandDisseminated Sclerosis with Narcolepsy (C565621)
..expandIrresistible sleepiness, cataplexy and onset of sleep in desynchronized phase (C538497)
..expandNarcolepsy 1 (C563534)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1804
Name:Cataplexy
Definition:A condition characterized by transient weakness or paralysis of somatic musculature triggered by an emotional stimulus or physical exertion. Cataplexy is frequently associated with NARCOLEPSY. During a cataplectic attack, there is a marked reduction in muscle tone similar to the normal physiologic hypotonia that accompanies rapid eye movement sleep (SLEEP, REM). (From Adams et al., Principles of Neurology, 6th ed, p396)
Alternative IDs:
ParentIDs:MESH:D009290
TreeNumbers:C10.886.425.800.200.750.500 |F03.870.400.800.200.750.500
Synonyms:Attack, Cataleptic |Attacks, Cataleptic |Cataleptic Attack |Cataleptic Attacks |Henneberg Syndrome |Status Cataplexicus |Syndrome, Henneberg |Syndromes, Tonelessness |Syndrome, Tonelessness |Tonelessness Syndrome |Tonelessness Syndromes
Slim Mappings:Mental disorder|Nervous system disease
Reference: MedGen: D002385
MeSH: D002385
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants