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Details
Link-It Detail - Human Phenotype - Abnormality of pain sensation
Debug Stats
  • ### Total Build Time: 46 ms 29.162 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 204 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 526 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=4 ms Completed: 4 ms rowSize= 783 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.084 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 3.018 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 22.415 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.023 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of pain sensation HP:0010832
Definition (1)
Pain is an unpleasant sensation that can range from mild, localized discomfort to agony, whereby the physical part of pain results from nerve stimulation and is often accompanied by an emotional component. This term groups abnormalities in pain sensation presumed to result from abnormalities related to the specific nerve fibers that carry the pain impulses to the brain.
Parents (2)
img Abnormality of the sensory nervous system HP:0001333
img Sensory impairment HP:0003474
Children (3)
img Trophic changes related to pain HP:0010834
img Impaired pain sensation HP:0007328
img Spontaneous pain sensation HP:0010833
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the sensory nervous system HP:0001333
img All HP:0000001img Phenotypic abnormality HP:00001187img Sensory impairment HP:0003474
img All HP:0000001img Phenotypic abnormality HP:00001188img Sensory impairment HP:0003474
Genes (37)

Species:
human : 37
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanIH100188864Hemihypertrophy
img HP RolledUp, OMIM ID: 235000
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanSCA25338435spinocerebellar ataxia 25
img HP RolledUp, OMIM ID: 608703
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP RolledUp, OMIM ID: 176270
HumanSHANK385358SH3 and multiple ankyrin repeat domains 3
img HP RolledUp, OMIM ID: 606232
HumanMAGEL254551MAGE-like 2
img HP RolledUp, OMIM ID: 176270
HumanNPAP123742nuclear pore associated protein 1
img HP RolledUp, OMIM ID: 176270
HumanCCT522948chaperonin containing TCP1, subunit 5 (epsilon)
img HP RolledUp, OMIM ID: 256840
HumanRAI110743retinoic acid induced 1
img HP RolledUp, OMIM ID: 182290
HumanMKRN3-AS110108
img HP RolledUp, OMIM ID: 176270
HumanHDAC49759histone deacetylase 4
img HP RolledUp, OMIM ID: 600430
HumanAIFM19131apoptosis-inducing factor, mitochondrion-associated, 1
img HP RolledUp, OMIM ID: 310490
HumanHERC28924HECT and RLD domain containing E3 ubiquitin protein ligase 2
img HP RolledUp, OMIM ID: 176270
HumanIKBKAP8518inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
img HP RolledUp, OMIM ID: 223900
HumanMKRN37681makorin ring finger protein 3
img HP RolledUp, OMIM ID: 176270
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
img HP RolledUp, OMIM ID: 176270
HumanSCN9A6335sodium channel, voltage-gated, type IX, alpha subunit
img HP RolledUp, OMIM ID: 243000
img HP RolledUp, OMIM ID: 167400
HumanPRPS15631phosphoribosyl pyrophosphate synthetase 1
img HP RolledUp, OMIM ID: 311070
HumanNTRK14914neurotrophic tyrosine kinase, receptor, type 1
img HP RolledUp, OMIM ID: 256800
HumanNOTCH34854notch 3
img HP RolledUp, OMIM ID: 125310
HumanNGF4803nerve growth factor (beta polypeptide)
img HP RolledUp, OMIM ID: 608654
HumanNDN4692necdin, melanoma antigen (MAGE) family member
img HP RolledUp, OMIM ID: 176270
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010832Abnormality of pain sensation0self