Myokymia
Symptom Information:
| Symptom ID: | HPO:0002411 | ||||
| Synonyms: |
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| Quality: | |||||
| 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) Abnormality of movement(HPO:0100022) Myokymia(HPO:0002411) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Muscle related signs and symptoms NEC(MedDRA:10028326) Myokymia(HPO:0002411) |
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| Database Frequency: | 10 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Autosomal recessive axonal neuropathy with neuromyotonia | (Orphanet:324442) |
| Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
| Benign familial neonatal seizures | (Orphanet:1949) |
| EPISODIC ATAXIA, TYPE 8 | (OMIM:616055) |
| Early-onset progressive neurodegeneration - blindness - ataxia - spasticity | (Orphanet:352654) |
| Episodic ataxia type 1 | (Orphanet:37612) |
| Episodic ataxia type 3 | (Orphanet:79135) |
| PAROXYSMAL NONKINESIGENIC DYSKINESIA 1 | (OMIM:118800) |
| Paroxysmal non-kinesigenic dyskinesia | (Orphanet:98810) |
| SEIZURES, BENIGN FAMILIAL NEONATAL, 1 | (OMIM:121200) |