Dysmetria

Symptom Information:

Symptom ID: HPO:0001310
Synonyms:
Dysmetria (finding) [Orphanet:43320]
Cerebellar Dysmetria [Orphanet:43320]
Dysmetria [OMIM:Dysmetria]
Execution movement disorder/dysmetria/bradykinesia/akinesia/apraxia [Orphanet:43320]
Dysmetria [Orphanet:43320]
Cerebellar syndrome [MedDRA:10008072]
Adiadokokinesis [MedDRA:10008072]
Dysdiadochokinesis [MedDRA:10008072]
Dysdiadokokinesis [MedDRA:10008072]
Dysmetria [MedDRA:10008072]
Syndrome cerebellar [MedDRA:10008072]
Dysdiadochokinesis (63%) [OMIM:Dysdiadochokinesis (63%)]
Dysmetria (1 patient) [OMIM:Dysmetria (1 patient)]
Dysmetria (in 1 of 3 families) [OMIM:Dysmetria (in 1 of 3 families)]
Dysmetria (type I) [OMIM:Dysmetria (type I)]
Execution movement disorder [Orphanet:43320]
Quality:
Cross references:
Orphanet:43320 "Execution movement disorder/dysmetria/bradykinesia/akinesia/apraxia" [Orphanet:43320]
OMIM: "Dysmetria" [OMIM:Dysmetria]
OMIM: "Dysdiadochokinesis (63%)" [OMIM:Dysdiadochokinesis (63%)]
OMIM: "Dysmetria (1 patient)" [OMIM:Dysmetria (1 patient)]
OMIM: "Dysmetria (in 1 of 3 families)" [OMIM:Dysmetria (in 1 of 3 families)]
OMIM: "Dysmetria (type I)" [OMIM:Dysmetria (type I)]
UMLS:C0234162 "Dysmetria" [HPO:0001310]
UMLS:C0234162 "Cerebellar Dysmetria" [Orphanet:43320]
Is a (Direct Parents):
Orphanet [DEL]Motor deficit/trouble
HPO         Ataxia
MedDRA Coordination and balance disturbances
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 central motor function(HPO:0011442)
                Abnormality of coordination(HPO:0011443)
                   Ataxia(HPO:0001251)
                      Dysmetria(HPO:0001310)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Coordination and balance disturbances(MedDRA:10072984)
          Dysmetria(HPO:0001310)
Database Frequency: 76 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION (OMIM:270500)
ATAXIA-OCULOMOTOR APRAXIA 3 (OMIM:615217)
Aceruloplasminemia (Orphanet:48818)
Adult-onset autosomal recessive cerebellar ataxia (Orphanet:284289)
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency (Orphanet:329314)
Alpha-mannosidosis (Orphanet:61)
Ataxia - pancytopenia (Orphanet:2585)
Autosomal recessive ataxia, Beauce type (Orphanet:88644)
Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome (Orphanet:363429)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency (Orphanet:324262)
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (Orphanet:98)
Autosomal recessive spastic ataxia with leukoencephalopathy (Orphanet:314603)
Autosomal recessive spastic paraplegia type 20 (Orphanet:101000)
Autosomal recessive spastic paraplegia type 26 (Orphanet:101006)
Autosomal recessive spastic paraplegia type 30 (Orphanet:101010)
Autosomal recessive spastic paraplegia type 35 (Orphanet:171629)
Autosomal recessive spastic paraplegia type 44 (Orphanet:320401)
Autosomal recessive spastic paraplegia type 48 (Orphanet:306511)
Autosomal recessive spastic paraplegia type 49 (Orphanet:320385)
CADASIL (Orphanet:136)
CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURALHEARING LOSS (OMIM:601338)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME1 (OMIM:224050)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 (OMIM:610185)
CLN5 disease (Orphanet:228360)
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA (OMIM:614306)
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18 (OMIM:615578)
Dysequilibrium syndrome (Orphanet:1766)
EPILEPSY, PROGRESSIVE MYOCLONIC, 1B (OMIM:612437)
EPILEPSY, PROGRESSIVE MYOCLONIC, 5 (OMIM:613832)
Early-onset progressive neurodegeneration - blindness - ataxia - spasticity (Orphanet:352654)
Early-onset spastic ataxia-neuropathy syndrome (Orphanet:313772)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Fucosidosis (Orphanet:349)
HERNS syndrome (Orphanet:63261)
Huntington disease-like 1 (Orphanet:157941)
Infantile-onset autosomal recessive nonprogressive cerebellar ataxia (Orphanet:284332)
LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY (OMIM:606183)
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM (OMIM:614381)
LEUKODYSTROPHY, HYPOMYELINATING, 9 (OMIM:616140)
LICHTENSTEIN-KNORR SYNDROME (OMIM:616291)
Leukoencephalopathy - ataxia - hypodontia - hypomyelination (Orphanet:137639)
MELAS (Orphanet:550)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
Mitochondrial myopathy - lactic acidosis - deafness (Orphanet:2597)
Moebius syndrome (Orphanet:570)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217)
Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency (Orphanet:88639)
Non-progressive cerebellar ataxia with intellectual deficit (Orphanet:314647)
Odontoleukodystrophy (Orphanet:77295)
Ornithine transcarbamylase deficiency (Orphanet:664)
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME (OMIM:606721)
PEROXISOME BIOGENESIS DISORDER 5B (OMIM:614867)
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract (Orphanet:171848)
Pontine tegmental cap dysplasia (Orphanet:269229)
SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE (OMIM:611302)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17 (OMIM:616127)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 (OMIM:616204)
Sialidosis type 1 (Orphanet:812)
Spastic paraplegia type 2 (Orphanet:99015)
Spectrin-associated autosomal recessive cerebellar ataxia (Orphanet:352403)
Spinocerebellar ataxia type 1 (Orphanet:98755)
Spinocerebellar ataxia type 10 (Orphanet:98761)
Spinocerebellar ataxia type 12 (Orphanet:98762)
Spinocerebellar ataxia type 14 (Orphanet:98763)
Spinocerebellar ataxia type 17 (Orphanet:98759)
Spinocerebellar ataxia type 18 (Orphanet:98771)
Spinocerebellar ataxia type 2 (Orphanet:98756)
Spinocerebellar ataxia type 23 (Orphanet:101108)
Spinocerebellar ataxia type 29 (Orphanet:208513)
Spinocerebellar ataxia type 35 (Orphanet:276193)
Spinocerebellar ataxia type 5 (Orphanet:98766)
Spinocerebellar ataxia type 7 (Orphanet:94147)
X-linked Charcot-Marie-Tooth disease type 1 (Orphanet:101075)
X-linked sideroblastic anemia - ataxia (Orphanet:2802)
X-linked spinocerebellar ataxia type 3 (Orphanet:85297)