Myoclonic spasms
Symptom Information:
Symptom ID: | HPO:0003739 | ||||||||||
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 musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Involuntary movements(HPO:0004305) Myoclonus(HPO:0001336) Myoclonic spasms(HPO:0003739) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Involuntary movements(HPO:0004305) Myoclonus(HPO:0001336) Myoclonic spasms(HPO:0003739) MedDRA: |
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Database Frequency: | 7 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Buschke-Ollendorff syndrome | (Orphanet:1306) |
MELAS | (Orphanet:550) |
RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL | (OMIM:614498) |
Stiff person syndrome | (Orphanet:3198) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |
Wolfram syndrome 1 | (OMIM:222300) |