| children | - [X]Other epilepsy 194491006 removed: 2009-01-31
- [X]Other generalized epilepsy and epileptic syndromes 194490007 removed: 2009-01-31
- [X]Other status epilepticus 194492004 removed: 2009-01-31
- [X]Status epilepticus, unspecified 194499008 removed: 2009-01-31
- Acquired epileptic aphasia 230438007
- Acute encephalopathy with biphasic seizures and late reduced diffusion 766044005
- Alopecia, epilepsy, intellectual disability syndrome Moynahan type 788417006
- Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome 720519003
- Atonic epilepsy 8291000119107 removed: 2023-05-31
- Atypical absence epilepsy 187931000119106 removed: 2021-09-30
- Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency 771448004
- Autism spectrum disorder, epilepsy, arthrogryposis syndrome 733623005
- Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency 770898002
- Benign adult familial myoclonic epilepsy 717225001
- Benign familial infantile epilepsy 1237571004
- Benign familial neonatal-infantile seizures 1231282002
- Benign infantile focal epilepsy with midline spikes and waves during sleep 770622009
- Benign infantile seizure with mild gastroenteritis syndrome 765756007
- Benign neonatal convulsions 38281008
- Celiac disease with epilepsy and cerebral calcification syndrome 722386009
- Centrencephalic epilepsy 49776008 removed: 2023-05-31
- Combined focal and generalized epilepsy 1260117009
- Congenital muscular dystrophy with intellectual disability and severe epilepsy 782772000
- Cryptogenic late-onset epileptic spasms 778063003
- DEND syndrome 721088003
- Developmental and epileptic encephalopathy 1275631007
- Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome 782737003
- Drug-induced epilepsy 230441003
- Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome 1172593006
- Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome 1187042007
- Epilepsy co-occurrent and due to degenerative brain disorder 724988000
- Epilepsy co-occurrent and due to dementia 724992007
- Epilepsy co-occurrent and due to demyelinating disorder 724991000
- Epilepsy co-occurrent and due to mesial temporal sclerosis 724989008
- Epilepsy due to bacterial endocarditis 1163529009
- Epilepsy due to cerebrovascular accident 724787004
- Epilepsy due to congenital anomaly of brain 1260377005
- Epilepsy due to congenital infectious disease 1260374003
- Epilepsy due to glucose transporter protein type 1 deficiency syndrome 1260375002
- Epilepsy due to immune disorder 724990004
- Epilepsy due to infectious disease of central nervous system 724549005
- Epilepsy due to intracranial tumor 724789001
- Epilepsy due to parasitic disease 1163527006
- Epilepsy due to perinatal anoxic-ischemic brain injury 724786008
- Epilepsy due to perinatal cerebral ischemia 1260371006
- Epilepsy due to perinatal intraventricular hemorrhage 1260369006
- Epilepsy due to perinatal periventricular hemorrhage 1260370007
- Epilepsy due to Rasmussen syndrome 1260368003
- Epilepsy in mother complicating childbirth 10750951000119106
- Epilepsy in mother complicating pregnancy 100941000119100
- Epilepsy NOS 267593008 removed: 2010-01-31
- Epilepsy of infancy with migrating focal seizures 733195008
- Epilepsy telangiectasia syndrome 733032006
- Epilepsy undetermined whether focal or generalized 230435005 removed: 2023-05-31
- Epilepsy, microcephaly, skeletal dysplasia syndrome 733031004
- Epilepsy, not refractory 422513000 removed: 2023-05-31
- Epileptic dementia with behavioral disturbance 82381000119103
- Epileptic encephalopathy 723125008
- Familial infantile myoclonic epilepsy 784342008
- Fatty acyl-CoA reductase 1 deficiency 1237619001
- Female restricted epilepsy with intellectual disability syndrome 716706009
- Fit (in known epileptic) NOS 309847002 removed: 2010-01-31
- Generalized epilepsy 19598007
- Infant epilepsy with migrant focal crisis 724274009
- Infantile spasm and broad thumb syndrome 770438007
- Kohlschutter's syndrome 109478007
- Localization-related epilepsy 230381009
- Malignant migrating partial seizures of infancy 784345005
- Other forms of epilepsy 193020001 removed: 2010-01-31
- Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome 773497001
- Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome 1167371007
- Post infectious grand mal epilepsy 698764006
- Post-cerebrovascular accident epilepsy 698767004
- Post-traumatic epilepsy 75023009
- Progressive myoclonic epilepsy 267581004
- Psychosensory epilepsy 193002005
- Pyridoxal 5-phosphate dependent epilepsy 724576005
- Pyridoxine-dependent epilepsy 734434007
- Reflex epilepsy 79745005
- Refractory epilepsy 445355009 removed: 2023-05-31
- Scar epilepsy 322112361000132104
- SCN8A-related epilepsy with encephalopathy 765170001
- Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome 723676007
- Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract 1179282009
- Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006
- Status epilepticus 230456007
- SYNGAP1-related intellectual disability 780827006
- Tonic-clonic epilepsy 352818000 removed: 2023-05-31
- Visceral epilepsy 2198002
- Visual epilepsy 39194005
- West syndrome 28055006
- X-linked epilepsy with learning disability and behavior disorder syndrome 717223008
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