Atonic seizures
Symptom Information:
Symptom ID: | HPO:0010819 | |||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Generalized seizures(HPO:0002197) Atonic seizures(HPO:0010819) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Muscle tone abnormalities(MedDRA:10028343) Atonic seizures(HPO:0010819) Nervous system disorders(MedDRA:10029205) Seizures(HPO:0001250) Seizures and seizure disorders NEC(MedDRA:10039912) Atonic seizures(HPO:0010819) |
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Database Frequency: | 18 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
EPILEPSY, PROGRESSIVE MYOCLONIC, 1B | (OMIM:612437) |
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET | (OMIM:615369) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19 | (OMIM:615744) |
FEBRILE SEIZURES, FAMILIAL, 1 | (OMIM:121210) |
FEBRILE SEIZURES, FAMILIAL, 2 | (OMIM:602477) |
FEBRILE SEIZURES, FAMILIAL, 4 | (OMIM:604352) |
FEBRILE SEIZURES, FAMILIAL, 5 | (OMIM:609255) |
FEBRILE SEIZURES, FAMILIAL, 6 | (OMIM:609253) |
Female restricted epilepsy with intellectual deficit | (Orphanet:101039) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1 | (OMIM:604233) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2 | (OMIM:604403) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3 | (OMIM:611277) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7 | (OMIM:613863) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9 | (OMIM:616172) |
Generalized epilepsy with febrile seizures-plus context | (Orphanet:36387) |
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency | (Orphanet:83639) |
Progressive myoclonic epilepsy type 6 | (Orphanet:280620) |
X-linked intellectual disability, Hedera type | (Orphanet:93952) |