Clumsiness

Symptom Information:

Symptom ID: HPO:0002312
Synonyms:
Clumsiness [OMIM:Clumsiness]
Clumsiness (82%) [OMIM:Clumsiness (82%)]
Clumsiness (mild) [OMIM:Clumsiness (mild)]
Clumsiness [MedDRA:10009696]
Quality:
Cross references:
OMIM: "Clumsiness" [OMIM:Clumsiness]
OMIM: "Clumsiness (82%)" [OMIM:Clumsiness (82%)]
OMIM: "Clumsiness (mild)" [OMIM:Clumsiness (mild)]
UMLS:C0233844 "Clumsiness" [HPO:0002312]
Is a (Direct Parents):
MedDRA Dyskinesias and movement disorders NEC
HPO         Incoordination
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)
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)