Dysdiadochokinesis

Symptom Information:

Symptom ID: HPO:0002075
Synonyms:
Dysdiadochokinesia [HPO:0002075]
DYSDIADOCHOKINESIA [HPO:0002075]
Dysdiadochokinesia [OMIM:Dysdiadochokinesia]
Dysdiadochokinesis [OMIM:Dysdiadochokinesis]
Dysdiadochokinesis (63%) [OMIM:Dysdiadochokinesis (63%)]
Quality:
Cross references:
OMIM: "Dysdiadochokinesia" [OMIM:Dysdiadochokinesia]
OMIM: "Dysdiadochokinesis" [OMIM:Dysdiadochokinesis]
OMIM: "Dysdiadochokinesis (63%)" [OMIM:Dysdiadochokinesis (63%)]
UMLS:C0234979 "DYSDIADOCHOKINESIA" [HPO:0002075]
Is a (Direct Parents):
HPO         Ataxia
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)
                      Dysdiadochokinesis(HPO:0002075)
MedDRA:
Database Frequency: 40 / 7739
Resource:

All diseases associated with this symptom:

Ataxia-telangiectasia-like disorder (Orphanet:251347)
Autosomal dominant striatal neurodegeneration (Orphanet:228169)
Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome (Orphanet:363429)
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency (Orphanet:324262)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 48 (Orphanet:306511)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 (OMIM:213600)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME1 (OMIM:224050)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 (OMIM:610185)
CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE (OMIM:605388)
CLN5 disease (Orphanet:228360)
Dysequilibrium syndrome (Orphanet:1766)
EAST syndrome (Orphanet:199343)
Early-onset X-linked optic atrophy (Orphanet:98890)
Early-onset spastic ataxia-neuropathy syndrome (Orphanet:313772)
Erythrokeratodermia - ataxia (Orphanet:1955)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Friedreich ataxia (Orphanet:95)
Friedreich ataxia 1 (OMIM:229300)
Hyperlysinemia, type I (OMIM:238700)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM (OMIM:614381)
LICHTENSTEIN-KNORR SYNDROME (OMIM:616291)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
Moebius syndrome (Orphanet:570)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217)
Ornithine transcarbamylase deficiency (Orphanet:664)
SPINOCEREBELLAR ATAXIA 40 (OMIM:616053)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 (OMIM:616204)
Spastic ataxia with congenital miosis (Orphanet:1182)
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 18 (Orphanet:98771)
Spinocerebellar ataxia type 2 (Orphanet:98756)
Spinocerebellar ataxia type 29 (Orphanet:208513)
Spinocerebellar ataxia type 5 (Orphanet:98766)
X-linked sideroblastic anemia - ataxia (Orphanet:2802)