Disease Browser
Parent Node: Calcinosis (D002114) Parent Node: Epilepsy (D004827) ..Starting node .. Epilepsy occipital calcifications (C535496) Child Nodes:
Sister Nodes: ..AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency (C563876) ..Alopecia epilepsy oligophrenia syndrome of Moynahan (C537052) ..Alopecia, epilepsy, pyorrhea, mental subnormality (C537057) ..Amish Infantile Epilepsy Syndrome (C563799) ..Arthrogryposis epileptic seizures migrational brain disorder (C537442) ..Battaglia Neri syndrome (C537662) ..BETA-AMINO ACIDS, RENAL TRANSPORT OF (OMIM:109660) ..Borjeson-Forssman-Lehmann syndrome (C536575) ..Boudhina Yedes Khiari syndrome (C537939) ..CHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB (OMIM:613729) ..Coffin syndrome 1 (C536435) ..Developmental Delay, Epilepsy, and Neonatal Diabetes (C565253) ..Epilepsies, Myoclonic (D004831) 26 ..Epilepsies, Partial (D004828) 26 ..Epilepsy occipital calcifications (C535496) ..Epilepsy telangiectasia (C535497) ..Epilepsy, Benign Neonatal (D020936) 13 ..Epilepsy, Benign Neonatal, 1, And/Or Myokymia (C567743) ..Epilepsy, Female-Restricted, with Mental Retardation (C564715) ..Epilepsy, Generalized (D004829) 27 ..EPILEPSY, HOT WATER, 1 (OMIM:613339) ..EPILEPSY, HOT WATER, 2 (OMIM:613340) ..Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation (C565587) ..Epilepsy, Post-Traumatic (D004834) ..Epilepsy, Reflex (D020195) ..Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders (C564505) ..Fryns-Aftimos Syndrome (C565258) ..Gurrieri Sammito Bellussi syndrome (C537625) ..HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT (OMIM:300049) ..Hyperekplexia and Epilepsy (C564474) ..Kifafa seizure disorder (C537708) ..Kohlschutter Tonz syndrome (C537213) ..Kuzniecky syndrome (C538091) ..Landau-Kleffner Syndrome (D018887) ..Lennox Gastaut Syndrome (D065768) 1 ..MEHMO syndrome (C537451) ..MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 (OMIM:613443) ..Mental Retardation, Microcephaly, Epilepsy, And Coarse Face (C563342) ..Mental Retardation, X-Linked, Syndromic, Christianson Type (C567484) ..Mental Retardation, X-Linked, with Epilepsy (C564516) ..Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy (C567020) ..Pyridoxine-dependent epilepsy (C536254) ..Ramon Syndrome (C535285) ..Retinal Degeneration and Epilepsy (C564847) ..Rud Syndrome (C535878) ..Sandhaus Ben-Ami syndrome (C537233) ..Seizures (D012640) 40 ..Seizures, Febrile (D003294) 21 ..Spinocerebellar Ataxia with Epilepsy (C564395) ..Status Epilepticus (D013226) 1 ..Wittwer syndrome (C536737) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 3882
Name: Epilepsy occipital calcifications
Definition:
Alternative IDs:
ParentIDs: MESH:D002114|MESH:D004827
TreeNumbers: C10.228.140.490/C535496 |C18.452.174.130/C535496
Synonyms: Bilateral occipital calcifications with epilepsy |Epilepsy with bilateral occipital calcifications |Familial unilateral and bilateral occipital calcifications and epilepsy
Slim Mappings: Metabolic disease|Nervous system disease
Reference:
MedGen: C535496
MeSH: C535496
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants