Incoordination

Symptom Information:

Symptom ID: HPO:0002311
Synonyms:
Difficulties in coordination [HPO:0002311]
Incoordination of limb movements [HPO:0002311]
Limb incoordination [HPO:0002311]
Ataxia [Orphanet:43210]
Incoordination (finding) [Orphanet:43210]
Ataxia (finding) [Orphanet:43210]
Coordination problem (finding) [Orphanet:43210]
Abnormal coordination [Orphanet:43210]
Ataxic [Orphanet:43210]
Difficulties in coordination [OMIM:Difficulties in coordination]
Incoordination [OMIM:Incoordination]
Incoordination of limb movements [OMIM:Incoordination of limb movements]
Limb incoordination [OMIM:Limb incoordination]
Ataxia/incoordination/trouble of the equilibrium [Orphanet:43210]
Coordination abnormal [Orphanet:43210]
Coordination abnormal [MedDRA:10010947]
Astasia [MedDRA:10010947]
Asynergia [MedDRA:10010947]
Coordination abnormal NOS [MedDRA:10010947]
Coordination disturbance [MedDRA:10010947]
Coordination impaired [MedDRA:10010947]
Coordination was decreased [MedDRA:10010947]
Decrease in coordination [MedDRA:10010947]
Incoordination [MedDRA:10010947]
Instability station [MedDRA:10010947]
Lack of coordination [MedDRA:10010947]
Muscular incoordination [MedDRA:10010947]
One leg standing difficult [MedDRA:10010947]
Sense of position abnormal [MedDRA:10010947]
Station abnormal [MedDRA:10010947]
Ataxia [MedDRA:10003591]
Ataxia NEC [MedDRA:10003591]
Ataxic [MedDRA:10003591]
Ataxic gait [MedDRA:10003591]
Ataxia aggravated [MedDRA:10003591]
Dystaxia [MedDRA:10003591]
Spastic ataxia [MedDRA:10003591]
Sensory ataxia [MedDRA:10003591]
Ataxia (1 patient) [OMIM:Ataxia (1 patient)]
Ataxia (CVS+) [OMIM:Ataxia (CVS+)]
Ataxia (deletion patients) [OMIM:Ataxia (deletion patients)]
Ataxia (early-onset form) [OMIM:Ataxia (early-onset form)]
Ataxia (if untreated) [OMIM:Ataxia (if untreated)]
Ataxia (in some patients) [OMIM:Ataxia (in some patients)]
Ataxia (less common) [OMIM:Ataxia (less common)]
Ataxia (often) [OMIM:Ataxia (often)]
Ataxia (type I and type II, infantile and juvenile) [OMIM:Ataxia (type I and type II, infantile and juvenile)]
Ataxia (uncommon) [OMIM:Ataxia (uncommon)]
Ataxia, (1 family) [OMIM:Ataxia, (1 family)]
Ataxic gait (in some) [OMIM:Ataxic gait (in some)]
Ataxic gait (juvenile form) [OMIM:Ataxic gait (juvenile form)]
Sensory ataxia (less common) [OMIM:Sensory ataxia (less common)]
Balance disorder [MedDRA:10049848]
Impairment of balance (finding) [Orphanet:43210]
Problem with balance (finding) [Orphanet:43210]
Equilibration disorder [Orphanet:43210]
Dysequilibrium [Orphanet:43210]
Quality:
Cross references:
HPO:0001251 "Ataxia" [Orphanet:43210]
HPO:0002066 "Gait ataxia" [Orphanet:43210]
Orphanet:43210 "Ataxia/incoordination/trouble of the equilibrium" [Orphanet:43210]
OMIM: "Difficulties in coordination" [OMIM:Difficulties in coordination]
OMIM: "Incoordination" [OMIM:Incoordination]
OMIM: "Incoordination of limb movements" [OMIM:Incoordination of limb movements]
OMIM: "Limb incoordination" [OMIM:Limb incoordination]
OMIM: "Ataxia (1 patient)" [OMIM:Ataxia (1 patient)]
OMIM: "Ataxia (CVS+)" [OMIM:Ataxia (CVS+)]
OMIM: "Ataxia (deletion patients)" [OMIM:Ataxia (deletion patients)]
OMIM: "Ataxia (early-onset form)" [OMIM:Ataxia (early-onset form)]
OMIM: "Ataxia (if untreated)" [OMIM:Ataxia (if untreated)]
OMIM: "Ataxia (in some patients)" [OMIM:Ataxia (in some patients)]
OMIM: "Ataxia (less common)" [OMIM:Ataxia (less common)]
OMIM: "Ataxia (often)" [OMIM:Ataxia (often)]
OMIM: "Ataxia (type I and type II, infantile and juvenile)" [OMIM:Ataxia (type I and type II, infantile and juvenile)]
OMIM: "Ataxia (uncommon)" [OMIM:Ataxia (uncommon)]
OMIM: "Ataxia, (1 family)" [OMIM:Ataxia, (1 family)]
OMIM: "Ataxic gait (in some)" [OMIM:Ataxic gait (in some)]
OMIM: "Ataxic gait (juvenile form)" [OMIM:Ataxic gait (juvenile form)]
OMIM: "Sensory ataxia (less common)" [OMIM:Sensory ataxia (less common)]
UMLS:C0520966 "Incoordination" [HPO:0002311]
UMLS:C0520966 "Abnormal coordination" [Orphanet:43210]
UMLS:C0234366 "Ataxic" [Orphanet:43210]
UMLS:C0004134 "Ataxia" [Orphanet:43210]
UMLS:C0575090 "Equilibration disorder" [Orphanet:43210]
UMLS:C0281825 "Dysequilibrium" [Orphanet:43210]
Is a (Direct Parents):
Orphanet Ataxia
MedDRA Coordination and balance disturbances
Orphanet [DEL]Motor deficit/trouble
HPO         Abnormality of coordination
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)
                   Incoordination(HPO:0002311)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Coordination and balance disturbances(MedDRA:10072984)
          Incoordination(HPO:0002311)
Database Frequency: 84 / 7739
Resource:

All diseases associated with this symptom:

2q23.1 microdeletion syndrome (Orphanet:228402)
3-methylglutaconic aciduria type 1 (Orphanet:67046)
3-methylglutaconic aciduria type 3 (Orphanet:67047)
48,XXYY syndrome (Orphanet:10)
6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
Aceruloplasminemia (Orphanet:48818)
Adrenomyeloneuropathy (Orphanet:139399)
Argininemia (Orphanet:90)
Argininosuccinic aciduria (Orphanet:23)
Autosomal dominant dopa-responsive dystonia (Orphanet:98808)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
Autosomal recessive spastic paraplegia type 46 (Orphanet:320391)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
Bangstad syndrome (Orphanet:1227)
Bardet-Biedl syndrome (Orphanet:110)
CARASIL (Orphanet:199354)
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA (OMIM:614306)
CYCLIC VOMITING SYNDROME (OMIM:500007)
Carbamoylphosphate synthetase deficiency (Orphanet:147)
Cerebroretinal vasculopathy (Orphanet:3421)
Charcot-Marie-Tooth disease type 4F (Orphanet:99952)
Citrullinemia type I (Orphanet:247525)
Classic maple syrup urine disease (Orphanet:268145)
Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
DE SANCTIS-CACCHIONE SYNDROME (OMIM:278800)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD (OMIM:130950)
Familial dysautonomia (Orphanet:1764)
Familial infantile myoclonic epilepsy (Orphanet:352582)
Friedreich ataxia 1 (OMIM:229300)
Friedreich ataxia 2 (OMIM:601992)
HERNS syndrome (Orphanet:63261)
Hereditary vascular retinopathy (Orphanet:71291)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency (Orphanet:395)
Huntington disease (Orphanet:399)
Huntington disease-like 1 (Orphanet:157941)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Juvenile Huntington disease (Orphanet:248111)
Kearns-Sayre syndrome (Orphanet:480)
Leber hereditary optic neuropathy (Orphanet:104)
Leigh syndrome (Orphanet:506)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO (OMIM:126200)
Maple syrup urine disease (Orphanet:511)
Maternally-inherited diabetes and deafness (Orphanet:225)
Methylmalonic acidemia with homocystinuria (Orphanet:26)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (Orphanet:369897)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Myopathy and diabetes mellitus (Orphanet:2596)
NARP syndrome (Orphanet:644)
NIEMANN-PICK DISEASE, TYPE C1 (OMIM:257220)
NIEMANN-PICK DISEASE, TYPE C2 (OMIM:607625)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
Niemann-Pick disease type C (Orphanet:646)
ORAL SENSIBILITY, DISTURBANCE OF (OMIM:258800)
Perrault Syndrome 1 (OMIM:233400)
Phosphoribosylpyrophosphate synthetase superactivity (Orphanet:3222)
Pitt-Hopkins syndrome (Orphanet:2896)
Pyruvate dehydrogenase E2 deficiency (Orphanet:79244)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 (OMIM:616204)
Sialidosis type 1 (Orphanet:812)
Spinocerebellar ataxia type 10 (Orphanet:98761)
Spinocerebellar ataxia type 26 (Orphanet:101112)
Spinocerebellar ataxia type 35 (Orphanet:276193)
Spinocerebellar ataxia type 36 (Orphanet:276198)
Spinocerebellar ataxia type 5 (Orphanet:98766)
Spinocerebellar ataxia type 8 (Orphanet:98760)
Sporadic Leigh syndrome (Orphanet:255199)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Transcobalamin deficiency (Orphanet:859)
Tyrosinemia type 2 (Orphanet:28378)
Williams syndrome (Orphanet:904)
Wilson-Turner syndrome (Orphanet:3459)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 1 (OMIM:222300)
X-linked Charcot-Marie-Tooth disease type 1 (Orphanet:101075)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)
X-linked spinocerebellar ataxia type 3 (Orphanet:85297)
Xeroderma pigmentosum complementation group F (Orphanet:276264)
[DEL] LEBER OPTIC ATROPHY (OMIM:535000)