Clumsiness
Symptom Information:
Symptom ID: | HPO:0002312 | ||||
Synonyms: |
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Quality: | |||||
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) Clumsiness(HPO:0002312) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Dyskinesias and movement disorders NEC(MedDRA:10013929) Clumsiness(HPO:0002312) |
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Database Frequency: | 28 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION | (OMIM:270500) |
Adult-onset dystonia-parkinsonism | (Orphanet:199351) |
Angelman syndrome | (Orphanet:72) |
Argininemia | (Orphanet:90) |
Argininosuccinic aciduria | (Orphanet:23) |
Autosomal dominant cervical dystonia | (Orphanet:93962) |
Autosomal dominant focal dystonia, DYT7 type | (Orphanet:93963) |
Autosomal recessive limb girdle muscular dystrophy type 2A | (Orphanet:267) |
BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
BROWN-VIALETTO-VAN LAERE SYNDROME 2 | (OMIM:614707) |
Benign paroxysmal tonic upgaze of childhood with ataxia | (Orphanet:1179) |
CHROMOSOME 15q11.2 DELETION SYNDROME | (OMIM:615656) |
CLN5 disease | (Orphanet:228360) |
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia | (Orphanet:284324) |
Classical phenylketonuria | (Orphanet:79254) |
Friedreich ataxia 1 | (OMIM:229300) |
Huntington disease | (Orphanet:399) |
Hyperlysinemia, type I | (OMIM:238700) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Infantile-onset autosomal recessive nonprogressive cerebellar ataxia | (Orphanet:284332) |
MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING,WITH OR WITHOUT MENTAL RETARDATION | (OMIM:613926) |
MYOPATHY, DISTAL, 3 | (OMIM:610099) |
Moebius syndrome | (Orphanet:570) |
Progressive epilepsy-intellectual deficit, Finnish type | (Orphanet:1947) |
Recessive mitochondrial ataxia syndrome | (Orphanet:94125) |
Riboflavin transporter deficiency | (Orphanet:97229) |
TENORIO SYNDROME | (OMIM:616260) |