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Details
Link-It Detail - Human Phenotype - Abnormality of the lower motor neuron
Debug Stats
  • ### Total Build Time: 36 ms 12.331 KB
  • CONCEPT_NAME gt=13 ms Completed: 13 ms rowSize= 212 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 210 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=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_NAMESPACE gt=NONE 1 ms Completed: 1 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 800 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 449 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 2.113 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 7.410 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.031 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the lower motor neuron HP:0002366
Definition (1)
An abnormality of the ` lower motor neuron` (FMA:84632).
Parents (2)
img Abnormality of the peripheral nervous system HP:0000759
img Abnormality of the motor neurons HP:0002450
Children (1)
img Lower motor neuron disease HP:0007276
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the peripheral nervous system HP:0000759
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the motor neurons HP:0002450
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanC9orf72203228chromosome 9 open reading frame 72
img HP IEA, OMIM ID: 105550
HumanC19orf1283636chromosome 19 open reading frame 12
img HP IEA, OMIM ID: 614298
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
img HP IEA, OMIM ID: 205100
img HP IEA, OMIM ID: 607225
HumanPLEKHG557449pleckstrin homology domain containing, family G (with RhoGef domain) member 5
img HP TAS, OMIM ID: 611067
HumanTRPM754822transient receptor potential cation channel, subfamily M, member 7
img HP TAS, OMIM ID: 105500
HumanSETX23064senataxin
img HP IEA, OMIM ID: 602433
HumanSIGMAR110280sigma non-opioid intracellular receptor 1
img HP IEA, OMIM ID: 614373
HumanDCTN11639dynactin 1
img HP IEA, OMIM ID: 607641
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002366Abnormality of the lower motor neuron0self