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Details
Link-It Detail - Human Phenotype - Abnormality of central motor function
Debug Stats
  • ### Total Build Time: 43 ms 21.763 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 212 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_GENES gt=32 ms Completed: 32 ms rowSize= 15.221 KB
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  • Reload Stats
Human Phenotype (1)
Abnormality of central motor function HP:0011442
Definition (1)
An anomaly of the control or production of movement in the central nervous system.
Parents (1)
img Abnormality of the central nervous system HP:0002011
Children (10)
img Central hypotonia HP:0011398
img Apraxia HP:0002186
img Spasmodic torticollis HP:0000473
img Abnormality of extrapyramidal motor function HP:0002071
img Paralysis HP:0003470
img Rigidity HP:0002063
img Abnormality of pyramidal motor function HP:0007256
img Cerebral palsy HP:0100021
img Abnormality of central motor conduction HP:0012079
img Abnormality of coordination HP:0011443
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the central nervous system HP:0002011
Genes (909)

Species:
human : 909
Page Size
Current 25
  Page 1 of 37
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSPG43101234260spastic paraplegia 43 (autosomal recessive)
img HP RolledUp, OMIM ID: 615043
HumanHMSN5101059903Hereditary motor and sensory neuropathy V
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
HumanSCAR12100820764Spinocerebellar ataxia, autosomal recessive 12
HumanMRXSCS100820761Mental retardation, X-linked, syndromic, Chudley-Schwartz type
HumanCCCSX100820758Cerebral-cerebellar-coloboma syndrome, X-linked
img HP RolledUp, OMIM ID: 300864
HumanDEL2Q23.1100820633
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
HumanSCA34100750330spinocerebellar ataxia 34
HumanTET18P100750329Tetrasomy 18p
HumanDEL3PTERP251006533853p- syndrome
HumanDEL17P13.1100653374
HumanOCLN100506658occludin
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
HumanDEL6Q24Q25100505391Chromosome 6q25-q25 deletion syndrome
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL17Q23.1Q23.2100415941
HumanSPAX3100379201Ataxia, spastic, 3, autosomal recessive
HumanSPG41100359402spastic paraplegia 41 (autosomal dominant)
HumanSPG45100322879spastic paraplegia 45 (autosomal recessive)
HumanGRD1100312954Graves disease, susceptiblity to, 1
HumanSCA31100312950spinocerebellar ataxia 31
HumanHTGH100302716Hypertrichosis terminalis, generalized, with or without gingival hyperplasia
HumanLKMCD100302058Leukoencephalopathy with metaphyseal chondrodysplasia
HumanDEL9P100240748Chromosome 9p deletion syndrome
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011442Abnormality of central motor function0self