Focal seizures with impairment of consciousness or awareness

Symptom Information:

Symptom ID: HPO:0002384
Synonyms:
Complex focal seizures [HPO:0002384]
Complex partial seizures [HPO:0002384]
Dyscognitive seizures [HPO:0002384]
Complex partial seizures [OMIM:Complex partial seizures]
Complex partial seizures (in some patients) [OMIM:Complex partial seizures (in some patients)]
Partial complex seizures [OMIM:Partial complex seizures]
Seizures, complex partial [OMIM:Seizures, complex partial]
Seizures, partial complex (rare) [OMIM:Seizures, partial complex (rare)]
Partial complex seizures [MedDRA:10034057]
Complex partial seizures [MedDRA:10010145]
Quality:
Cross references:
OMIM: "Complex partial seizures" [OMIM:Complex partial seizures]
OMIM: "Complex partial seizures (in some patients)" [OMIM:Complex partial seizures (in some patients)]
OMIM: "Partial complex seizures" [OMIM:Partial complex seizures]
OMIM: "Seizures, complex partial" [OMIM:Seizures, complex partial]
OMIM: "Seizures, partial complex (rare)" [OMIM:Seizures, partial complex (rare)]
Is a (Direct Parents):
HPO         Focal seizures
HPO         Dialeptic seizures
MedDRA Seizures
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)