Dysmetria
Symptom Information:
Symptom ID: | HPO:0001310 | ||||||||||||||||
Synonyms: |
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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 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) |
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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) |