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Details
Link-It Detail - Human Phenotype - Abnormality of the corticospinal tract
Debug Stats
  • ### Total Build Time: 35 ms 30.542 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 213 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=1 ms Completed: 1 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= 456 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 3.475 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.107 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=21 ms Completed: 21 ms rowSize= 23.130 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.032 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the corticospinal tract HP:0002492
Parents (1)
img Abnormality of the pyramidal tracts HP:0002062
Children (10)
img Corticospinal tract disease in lower limbs HP:0007163
img Aplasia/Hypoplasia involving the corticospinal tracts HP:0007365
img Babinski sign HP:0003487
img Dysfunction of lateral corticospinal tracts HP:0007299
img Corticospinal tract dysfunction HP:0002493
img Atrophy/Degeneration involving the corticospinal tracts HP:0007372
img Early involvement of the corticospinal pathways HP:0006912
img Corticospinal tract pallor HP:0008361
img Pathologic changes in anterior horn cells and lateral corticospinal tracts HP:0007254
img Corticospinal signs HP:0007225
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
Genes (145)

Species:
human : 145
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSPG43101234260spastic paraplegia 43 (autosomal recessive)
img HP RolledUp, OMIM ID: 615043
HumanHMSN5101059903Hereditary motor and sensory neuropathy V
img HP RolledUp, OMIM ID: 600361
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanSPG45100322879spastic paraplegia 45 (autosomal recessive)
img HP RolledUp, OMIM ID: 613162
HumanLKMCD100302058Leukoencephalopathy with metaphyseal chondrodysplasia
img HP RolledUp, OMIM ID: 300660
HumanPLSA1100240702Primary lateral sclerosis, adult, 1
img HP RolledUp, OMIM ID: 611637
HumanSAX2100126095spastic ataxia 2 (autosomal recessive)
img HP RolledUp, OMIM ID: 611302
HumanSPG38100049707spastic paraplegia 38 (autosomal dominant, Silver syndrome)
img HP RolledUp, OMIM ID: 612335
HumanSPG37100049159spastic paraplegia 37 (autosomal dominant)
img HP RolledUp, OMIM ID: 611945
HumanSPG36791228spastic paraplegia 36 (autosomal dominant)
img HP RolledUp, OMIM ID: 613096
HumanSCAR7727719spinocerebellar ataxia, autosomal recessive 7
img HP RolledUp, OMIM ID: 609270
HumanSPG34724110spastic paraplegia 34 (autosomal dominant)
img HP RolledUp, OMIM ID: 300750
HumanSPG32724107spastic paraplegia 32 (autosomal recessive)
img HP RolledUp, OMIM ID: 611252
HumanSDHAF1644096succinate dehydrogenase complex assembly factor 1
img HP RolledUp, OMIM ID: 252011
HumanSPG29619379spastic paraplegia 29 (autosomal dominant)
img HP RolledUp, OMIM ID: 609727
HumanSPG26550623spastic paraplegia 26
img HP RolledUp, OMIM ID: 609195
HumanSNAX1474386sensory ataxia 1 (autosomal dominant)
img HP RolledUp, OMIM ID: 608984
HumanSPG27414886spastic paraplegia 27 (autosomal recessive)
img HP RolledUp, OMIM ID: 609041
HumanSPG23353293spastic paraplegia 23 (autosomal recessive)
img HP RolledUp, OMIM ID: 270750
HumanTGM6343641transglutaminase 6
img HP RolledUp, OMIM ID: 613908
HumanSCA25338435spinocerebellar ataxia 25
img HP RolledUp, OMIM ID: 608703
HumanSCASI260415spinocerebellar ataxia with saccadic intrusions
img HP RolledUp, OMIM ID: 607317
HumanPRICKLE1144165prickle homolog 1 (Drosophila)
img HP RolledUp, OMIM ID: 612437
HumanSPG19140907spastic paraplegia 19 (autosomal dominant)
img HP RolledUp, OMIM ID: 607152
HumanSPG18140906spastic paraplegia 18 (autosomal dominant)
img HP RolledUp, OMIM ID: 611225
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002492Abnormality of the corticospinal tract0self