Hypokinesia
Symptom Information:
Symptom ID: | HPO:0002375 | ||||||
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) 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) |
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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) |