Disease Browser
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Parent Node: Epilepsy (D004827) |
..Starting node ..EPILEPSY, HOT WATER, 2 (OMIM:613340)
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Child Nodes:
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Sister Nodes: |
..AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency (C563876)
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..Alopecia epilepsy oligophrenia syndrome of Moynahan (C537052)
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..Alopecia, epilepsy, pyorrhea, mental subnormality (C537057)
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..Amish Infantile Epilepsy Syndrome (C563799)
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..Arthrogryposis epileptic seizures migrational brain disorder (C537442)
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..Battaglia Neri syndrome (C537662)
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..BETA-AMINO ACIDS, RENAL TRANSPORT OF (OMIM:109660)
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..Borjeson-Forssman-Lehmann syndrome (C536575)
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..Boudhina Yedes Khiari syndrome (C537939)
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..CHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB (OMIM:613729)
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..Coffin syndrome 1 (C536435)
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..Developmental Delay, Epilepsy, and Neonatal Diabetes (C565253)
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..Epilepsies, Myoclonic (D004831) 26
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..Epilepsies, Partial (D004828) 26
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..Epilepsy occipital calcifications (C535496)
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..Epilepsy telangiectasia (C535497)
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..Epilepsy, Benign Neonatal (D020936) 13
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..Epilepsy, Benign Neonatal, 1, And/Or Myokymia (C567743)
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..Epilepsy, Female-Restricted, with Mental Retardation (C564715)
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..Epilepsy, Generalized (D004829) 27
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..EPILEPSY, HOT WATER, 1 (OMIM:613339)
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..EPILEPSY, HOT WATER, 2 (OMIM:613340)
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..Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation (C565587)
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..Epilepsy, Post-Traumatic (D004834)
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..Epilepsy, Reflex (D020195)
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..Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders (C564505)
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..Fryns-Aftimos Syndrome (C565258)
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..Gurrieri Sammito Bellussi syndrome (C537625)
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..HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT (OMIM:300049)
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..Hyperekplexia and Epilepsy (C564474)
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..Kifafa seizure disorder (C537708)
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..Kohlschutter Tonz syndrome (C537213)
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..Kuzniecky syndrome (C538091)
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..Landau-Kleffner Syndrome (D018887)
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..Lennox Gastaut Syndrome (D065768) 1
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..MEHMO syndrome (C537451)
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..MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 (OMIM:613443)
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..Mental Retardation, Microcephaly, Epilepsy, And Coarse Face (C563342)
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..Mental Retardation, X-Linked, Syndromic, Christianson Type (C567484)
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..Mental Retardation, X-Linked, with Epilepsy (C564516)
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..Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy (C567020)
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..Pyridoxine-dependent epilepsy (C536254)
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..Ramon Syndrome (C535285)
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..Retinal Degeneration and Epilepsy (C564847)
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..Rud Syndrome (C535878)
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..Sandhaus Ben-Ami syndrome (C537233)
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..Seizures (D012640) 40
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..Seizures, Febrile (D003294) 21
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..Spinocerebellar Ataxia with Epilepsy (C564395)
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..Status Epilepticus (D013226) 1
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..Wittwer syndrome (C536737)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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