Myoclonic spasms

Symptom Information:

Symptom ID: HPO:0003739
Synonyms:
SPASMS [HPO:0003739]
Myoclonic spasms [OMIM:Myoclonic spasms]
Muscle spasms [MedDRA:10028334]
Muscle contracture [Orphanet:44200]
Contracture (morphologic abnormality) [Orphanet:44200]
Spasm (finding) [Orphanet:44200]
Muscle contracture (disorder) [Orphanet:44200]
Contracture [Orphanet:44200]
Spasm [Orphanet:44200]
Contractures/cramps/trismus/tetania/claudication/opisthotonos [Orphanet:44200]
Quality:
Cross references:
Orphanet:44200 "Contractures/cramps/trismus/tetania/claudication/opisthotonos" [Orphanet:44200]
OMIM: "Myoclonic spasms" [OMIM:Myoclonic spasms]
UMLS:C0037763 "SPASMS" [HPO:0003739]
UMLS:C0009917 "Contracture" [Orphanet:44200]
UMLS:C0037763 "Spasm" [Orphanet:44200]
Is a (Direct Parents):
Orphanet Trismus
HPO         Myoclonus
Orphanet Muscle anomalies
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:
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)