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Details
Link-It Detail - Human Phenotype - Abnormal aggressive, impulsive or violent behavior
Debug Stats
  • ### Total Build Time: 40 ms 52.854 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 225 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 775 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.369 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=7 ms Completed: 7 ms rowSize= 26.079 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=21 ms Completed: 21 ms rowSize= 23.241 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.044 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal aggressive, impulsive or violent behavior HP:0006919
Parents (2)
img Aggressive behavior HP:0000718
img Abnormal emotion/affect behavior HP:0100851
Children (4)
img Aggressive behavior HP:0000718
img Violent behavior HP:0008760
img Self-injurious behavior HP:0100716
img Impulsivity HP:0100710
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:00001187img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:00001188img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:00001186img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011811img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011810img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011813img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011812img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011815img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011814img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011817img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011816img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011819img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011818img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011821img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011820img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011823img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011822img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011825img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011824img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011827img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011826img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011829img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011828img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011831img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:000011830img Aggressive behavior HP:0000718
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormal emotion/affect behavior HP:0100851
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormal emotion/affect behavior HP:0100851
Genes (109)

Species:
human : 109
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP RolledUp, OMIM ID: 612582
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanJAWAD100192306Microcephaly with digital anomalies
img HP RolledUp, OMIM ID: 251255
HumanDEL2Q32Q33100190983Chromosome 2q32-q33 deletion syndrome
img HP RolledUp, OMIM ID: 612313
HumanMICRODEL3Q29100188788Chromosome 3q29 microdeletion syndrome
img HP RolledUp, OMIM ID: 609425
HumanTQDS780911Chromosome 10q deletion syndrome
img HP RolledUp, OMIM ID: 609625
HumanDUPC1780895Dupuytren contracture 1
img HP RolledUp, OMIM ID: 126900
HumanWDR62284403WD repeat domain 62
img HP RolledUp, OMIM ID: 604317
HumanNAGS162417N-acetylglutamate synthase
img HP RolledUp, OMIM ID: 237310
HumanUROC1131669urocanate hydratase 1
img HP RolledUp, OMIM ID: 276880
HumanSLITRK1114798SLIT and NTRK-like family, member 1
img HP RolledUp, OMIM ID: 137580
HumanCEP4195681centrosomal protein 41kDa
img HP RolledUp, OMIM ID: 213300
HumanSHANK385358SH3 and multiple ankyrin repeat domains 3
img HP RolledUp, OMIM ID: 606232
HumanC19orf1283636chromosome 19 open reading frame 12
img HP RolledUp, OMIM ID: 614298
HumanTCTN279867tectonic family member 2
img HP RolledUp, OMIM ID: 213300
HumanEHMT179813euchromatic histone-lysine N-methyltransferase 1
img HP RolledUp, OMIM ID: 610253
HumanTTC21B79809tetratricopeptide repeat domain 21B
img HP RolledUp, OMIM ID: 213300
HumanTMEM23179583transmembrane protein 231
img HP RolledUp, OMIM ID: 614970
img HP RolledUp, OMIM ID: 213300
HumanSLC52A279581solute carrier family 52 (riboflavin transporter), member 2
img HP RolledUp, OMIM ID: 614707
HumanC5orf4265250chromosome 5 open reading frame 42
img HP RolledUp, OMIM ID: 213300
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0006919Abnormal aggressive, impulsive or violent behavior0self