Hypokinesia

Symptom Information:

Symptom ID: HPO:0002375
Synonyms:
Decreased spontaneous movement [HPO:0002375]
Decreased spontaneous movements [HPO:0002375]
Decreased spontaneous movement [OMIM:Decreased spontaneous movement]
Decreased spontaneous movements [OMIM:Decreased spontaneous movements]
Hypokinesia [OMIM:Hypokinesia]
Hypokinesia [MedDRA:10021021]
Quality:
Cross references:
OMIM: "Decreased spontaneous movement" [OMIM:Decreased spontaneous movement]
OMIM: "Decreased spontaneous movements" [OMIM:Decreased spontaneous movements]
OMIM: "Hypokinesia" [OMIM:Hypokinesia]
UMLS:C0086439 "Hypokinesia" [HPO:0002375]
Is a (Direct Parents):
HPO         Diminished movement
MedDRA Dyskinesias and movement disorders NEC
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)
                Diminished movement(HPO:0002374)
                   Hypokinesia(HPO:0002375)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Dyskinesias and movement disorders NEC(MedDRA:10013929)
          Hypokinesia(HPO:0002375)
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
Adenylosuccinate lyase deficiency (Orphanet:46)
Arrhythmogenic right ventricular dysplasia, familial, 4 (OMIM:602087)
Autosomal dominant striatal neurodegeneration (Orphanet:228169)
Autosomal recessive dopa-responsive dystonia (Orphanet:101150)
BROWN-VIALETTO-VAN LAERE SYNDROME 2 (OMIM:614707)
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis (OMIM:615821)
Combined oxidative phosphorylation defect type 2 (Orphanet:254920)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 (OMIM:616211)
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria (Orphanet:1035)
FETAL AKINESIA SYNDROME, X-LINKED (OMIM:300073)
Fetal Gaucher disease (Orphanet:85212)
Gaucher disease type 2 (Orphanet:77260)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hereditary hyperekplexia (Orphanet:3197)
Kufor-Rakeb syndrome (Orphanet:306674)
Leigh syndrome (Orphanet:506)
MUSCULAR HYPERTONIA, LETHAL (OMIM:254120)
NEMALINE MYOPATHY 8 (OMIM:615348)
Parkinsonim due to ATP13A2 deficiency (Orphanet:314632)
Severe X-linked mitochondrial encephalomyopathy (Orphanet:238329)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
X-linked centronuclear myopathy (Orphanet:596)
Young adult-onset Parkinsonism (Orphanet:2828)