Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Human Phenotype - Abnormality of movement
Debug Stats
  • ### Total Build Time: 145 ms 48.115 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 198 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 411 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=19 ms Completed: 19 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 792 bytes
  • CONCEPT_CHILDREN gt=30 ms Completed: 30 ms rowSize= 19.817 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 3.043 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=82 ms Completed: 82 ms rowSize= 22.725 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.018 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of movement HP:0100022
Definition (1)
Movement disorders are characterized by the phenotypic abnormalities including abnormal involuntary movements, akathisia, akinesia, athetosis, ataxia, ballismus, bradykinesia, chorea, dyskinesia, dystonia, and myoclonus tics, tremor, spasms, and stereotypy.
Parents (2)
img Behavioural/Psychiatric Abnormality HP:0000708
img Abnormality of the nervous system HP:0000707
Children (62)
img Abnormal head movements HP:0002457
img Scapulohumeral synostosis HP:0006595
img Parkinsonism HP:0001300
img Chorea HP:0002072
img Clonus HP:0002169
img Gower sign HP:0003391
img Limited shoulder movement HP:0006467
img Restricted chest movement HP:0006596
img Bradykinesia HP:0002067
img Diminished movement HP:0002374
img Movement abnormality of the tongue HP:0000182
img Cerebral palsy HP:0100021
img Ataxia HP:0001251
img Gait disturbance HP:0001288
img Incoordination HP:0002311
img Restricted large joint movement HP:0005193
img Involuntary rhythmic myoclonic movements ('tremor') of the distal extremities, usually fingers HP:0001295
img Hyperorality HP:0000710
img Restlessness HP:0000711
img Restricted neck movement due to contractures HP:0005997
img Decreased movement range in interphalangeal joints HP:0006203
img Abnormality of eye movement HP:0000496
img Hyperactivity HP:0000752
img Limited elbow movement HP:0002996
img Involuntary jerking movements HP:0007087
img Progressive extrapyramidal movement disorder HP:0007153
img Asterixis HP:0012164
img Tongue thrusting HP:0100703
img Movements ('tremors') characterized by 8 to 10-Hz discharges HP:0001309
img Abnormal posturing HP:0002533
img Limited interphalangeal movement HP:0006064
img Limited wrist movement HP:0006248
img Sprengel anomaly HP:0000912
img Postural instability HP:0002172
img Athetosis HP:0002305
img Orofacial dyskinesia HP:0002310
img Involuntary movements of extremities, neck, trunk, and/or face HP:0007120
img Myoclonus HP:0001336
img Frontal release signs HP:0000743
img Dystonia HP:0001332
img Tremor HP:0001337
img Prenatal movement abnormality HP:0001557
img Limited hip movement HP:0008800
img Tics HP:0100033
img Recurrent hand flapping HP:0100023
img Apraxia HP:0002186
img Myokymia HP:0002411
img Bimanual synkinesia HP:0001335
img Hyperkinesis HP:0002487
img Decreased spontaneous movements HP:0002603
img Exaggerated startle response HP:0002267
img Paralysis HP:0003470
img Limited knee movement HP:0005192
img Stereotypic behavior HP:0000733
img Fasciculations HP:0002380
img Involuntary movements HP:0004305
img Paroxysmal dyskinesia HP:0007166
img Extrapyramidal dyskinesia HP:0007308
img Involuntary writhing movements HP:0007316
img Limitation of movement at ankles HP:0010505
img Dyskinesia HP:0100660
img Muscle fibrillation HP:0010546
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Behavioural/Psychiatric Abnormality HP:0000708
img All HP:0000001img Phenotypic abnormality HP:00001185img Behavioural/Psychiatric Abnormality HP:0000708
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the nervous system HP:0000707
Genes (1402)

Species:
human : 1402
Page Size
Current 25
  Page 1 of 57
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSMAJ101241900Spinal muscular atrophy, Jokela type
img HP RolledUp, OMIM ID: 615048
HumanSPG43101234260spastic paraplegia 43 (autosomal recessive)
img HP RolledUp, OMIM ID: 615043
HumanHMSN5101059903Hereditary motor and sensory neuropathy V
HumanNYS7101055624Nystagmus 7, congenital
img HP RolledUp, OMIM ID: 614826
HumanDUP16P11.2100909384
img HP RolledUp, OMIM ID: 614671
HumanDELXQ21100887743Choroideremia, deafness, and mental retardation
img HP RolledUp, OMIM ID: 303110
HumanDYT21100885773dystonia 21, torsion (autosomal dominant)
img HP RolledUp, OMIM ID: 614588
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanSCAR12100820764Spinocerebellar ataxia, autosomal recessive 12
img HP RolledUp, OMIM ID: 614322
HumanMRXSCS100820761Mental retardation, X-linked, syndromic, Chudley-Schwartz type
img HP RolledUp, OMIM ID: 300861
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanSCA34100750330spinocerebellar ataxia 34
img HP RolledUp, OMIM ID: 133190
HumanTET18P100750329Tetrasomy 18p
img HP RolledUp, OMIM ID: 614290
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanDEL7Q11.23100653380
img HP RolledUp, OMIM ID: 613729
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanLCR-OPSIN100534624
HumanFAME3100529229Epilepsy, familial adult myoclonic, 3
img HP RolledUp, OMIM ID: 613608
HumanDUP17Q21.31100529226
img HP RolledUp, OMIM ID: 613533
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100022Abnormality of movement0self