Incoordination
Symptom Information:
Symptom ID: | HPO:0002311 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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 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) |
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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) |