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Details
Link-It Detail - Human Phenotype - Abnormality of pyramidal motor function
Debug Stats
  • ### Total Build Time: 48 ms 30.543 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 214 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 238 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
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  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 796 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.018 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 3.047 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=31 ms Completed: 31 ms rowSize= 23.082 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.033 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of pyramidal motor function HP:0007256
Definition (1)
Functional neurological abnormalities related to dysfunction of the pyramidal tract.
Parents (2)
img Abnormality of the pyramidal tracts HP:0002062
img Abnormality of central motor function HP:0011442
Children (6)
img Hypertonia HP:0001276
img Hyperreflexia HP:0001347
img Pyramidal signs, mild HP:0007324
img Babinski sign HP:0003487
img Paralysis due to lesions of the principle motor tracts HP:0010549
img Chaddock reflex HP:0010875
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the pyramidal tracts HP:0002062
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the pyramidal tracts HP:0002062
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of central motor function HP:0011442
Genes (631)

Species:
human : 631
Page Size
Current 25
  Page 1 of 26
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSPG43101234260spastic paraplegia 43 (autosomal recessive)
img HP RolledUp, OMIM ID: 615043
HumanHMSN5101059903Hereditary motor and sensory neuropathy V
img HP IEA, OMIM ID: 600361
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanTET18P100750329Tetrasomy 18p
img HP RolledUp, OMIM ID: 614290
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanOCLN100506658occludin
img HP RolledUp, OMIM ID: 251290
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP RolledUp, OMIM ID: 613457
HumanDEL6Q24Q25100505391Chromosome 6q25-q25 deletion syndrome
img HP RolledUp, OMIM ID: 612863
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanSPAX3100379201Ataxia, spastic, 3, autosomal recessive
img HP RolledUp, OMIM ID: 611390
HumanSPG41100359402spastic paraplegia 41 (autosomal dominant)
img HP RolledUp, OMIM ID: 613364
HumanSPG45100322879spastic paraplegia 45 (autosomal recessive)
img HP RolledUp, OMIM ID: 613162
HumanGRD1100312954Graves disease, susceptiblity to, 1
img HP RolledUp, OMIM ID: 275000
HumanLKMCD100302058Leukoencephalopathy with metaphyseal chondrodysplasia
img HP RolledUp, OMIM ID: 300660
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanPLSA1100240702Primary lateral sclerosis, adult, 1
img HP RolledUp, OMIM ID: 611637
HumanDUP1Q21100217371Chromosome 1q21.1 duplication syndrome
img HP RolledUp, OMIM ID: 612475
HumanMRT5100188831mental retardation, non-syndromic, autosomal recessive, 5
img HP RolledUp, OMIM ID: 611091
HumanCD24100133941CD24 molecule
HumanSAX2100126095spastic ataxia 2 (autosomal recessive)
img HP RolledUp, OMIM ID: 611302
HumanSPG38100049707spastic paraplegia 38 (autosomal dominant, Silver syndrome)
img HP RolledUp, OMIM ID: 612335
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0007256Abnormality of pyramidal motor function0self