Dysdiadochokinesis
Symptom Information:
Symptom ID: | HPO:0002075 | |||||
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) Ataxia(HPO:0001251) Dysdiadochokinesis(HPO:0002075) MedDRA: |
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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) |