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Parent Node:
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Epilepsy, Generalized (D004829)
..Starting node
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Spasms, Infantile (D013036)

       Child Nodes:
........expandConvulsions, Benign Familial Infantile, 2 (C565296)
........expandEpileptic Encephalopathy, Early Infantile, 1 (C567924)
........expandEpileptic Encephalopathy, Early Infantile, 2 (C564064)
........expandEpileptic Encephalopathy, Early Infantile, 3 (C562695)
........expandEpileptic Encephalopathy, Early Infantile, 4 (C567404)
........expandMicrocephaly, corpus callosum dysgenesis and cleft lip-palate (C537547)
........expandNorrie disease (C537849)
........expandPEHO syndrome (C536317)
........expandX-linked infantile spasm syndrome (C538670)



 Sister Nodes: 
..expandEpilepsy, Absence (D004832) Child1
..expandEpilepsy, Idiopathic Generalized (C562694)
..expandEpilepsy, Tonic-Clonic (D004830) Child1
..expandGeneralized Epilepsy and Paroxysmal Dyskinesia (C563719)
..expandGeneralized Epilepsy with Febrile Seizures Plus (C565808)
..expandGeneralized Epilepsy With Febrile Seizures Plus, 7 (C567827)
..expandGeneralized Epilepsy With Febrile Seizures Plus, Type 1 (C565809)
..expandGeneralized Epilepsy With Febrile Seizures Plus, Type 2 (C565810)
..expandGeneralized Epilepsy With Febrile Seizures Plus, Type 3 (C565811)
..expandGeneralized Epilepsy With Febrile Seizures Plus, Type 4 (C565227)
..expandGeneralized Epilepsy With Febrile Seizures Plus, Type 5 (C565812)
..expandGeneralized Epilepsy With Febrile Seizures Plus, Type 6 (C567371)
..expandGENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 8 (OMIM:613828)
..expandNodding Syndrome (D064128)
..expandPHOTOPAROXYSMAL RESPONSE 2 (OMIM:609572)
..expandSpasms, Infantile (D013036) Child9
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:10353
Name:Spasms, Infantile
Definition:An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)
Alternative IDs:
ParentIDs:MESH:D004829
TreeNumbers:C10.228.140.490.375.760
Synonyms:Attack, Lightning |Attacks, Lightning |Attacks, Salaam |Cryptogenic Infantile Spasm |Cryptogenic Infantile Spasms |Cryptogenic West Syndrome |Hypsarrhythmia |Hypsarrhythmias |Infantile Spasm |Infantile Spasm, Cryptogenic |Infantile Spasms |Infantile Spasms, Cryptog
Slim Mappings:Nervous system disease
Reference: MedGen: D013036
MeSH: D013036
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants