Focal seizures with impairment of consciousness or awareness
Symptom Information:
Symptom ID: | HPO:0002384 | ||||||||||
Synonyms: |
|
||||||||||
Quality: | |||||||||||
Cross references: |
|
||||||||||
Is a (Direct Parents): |
|
||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Seizures(HPO:0001250) Dialeptic seizures(HPO:0011146) Focal seizures with impairment of consciousness or awareness(HPO:0002384) Focal seizures(HPO:0007359) Focal seizures with impairment of consciousness or awareness(HPO:0002384) MedDRA: Nervous system disorders(MedDRA:10029205) Seizures(HPO:0001250) Focal seizures with impairment of consciousness or awareness(HPO:0002384) |
||||||||||
Database Frequency: | 17 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
APNEA, OBSTRUCTIVE SLEEP | (OMIM:107650) |
Aldosterone-producing adenoma with seizures and neurological abnormalities | (Orphanet:369929) |
Autosomal dominant epilepsy with auditory features | (Orphanet:101046) |
Benign familial mesial temporal lobe epilepsy | (Orphanet:163717) |
Dravet syndrome | (Orphanet:33069) |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 | (OMIM:608096) |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 4 | (OMIM:611631) |
Familial temporal epilepsy | (Orphanet:98819) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9 | (OMIM:616172) |
Isolated focal cortical dysplasia type II | (Orphanet:268994) |
Leukoencephalopathy - ataxia - hypodontia - hypomyelination | (Orphanet:137639) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47 | (OMIM:616193) |
Mitochondrial myopathy - lactic acidosis - deafness | (Orphanet:2597) |
Odontoleukodystrophy | (Orphanet:77295) |
POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL | (OMIM:612691) |
Progressive epilepsy-intellectual deficit, Finnish type | (Orphanet:1947) |