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Details
Link-It Detail - Human Phenotype - Abnormal emotion/affect behavior
Debug Stats
  • ### Total Build Time: 45 ms 35.114 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 207 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 192 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= 456 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 8.010 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.107 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=29 ms Completed: 29 ms rowSize= 22.991 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal emotion/affect behavior HP:0100851
Definition (1)
An abnormality of emotional behaviour.
Parents (1)
img Behavioural/Psychiatric Abnormality HP:0000708
Children (25)
img Low frustration tolerance HP:0000744
img Depression HP:0000716
img Apathy HP:0000741
img Pseudobulbar behavioral symptoms HP:0002193
img Anhedonia HP:0012154
img Restlessness HP:0000711
img Lack of spontaneous play HP:0000721
img Aggressive behavior HP:0000718
img Autism spectrum disorder HP:0000729
img Autism HP:0000717
img Abnormal aggressive, impulsive or violent behavior HP:0006919
img Echolalia HP:0010529
img Lack of motivation HP:0000745
img Inappropriate behavior HP:0000719
img Lack of insight HP:0000757
img Restrictive behavior HP:0000723
img Mutism HP:0002300
img Oppositional defiant disorder HP:0010865
img Abnormal fear/anxiety-related behavior HP:0100852
img Inflexible adherence to routines or rituals HP:0000732
img Irritability HP:0000737
img Overfriendliness HP:0100025
img Conspicuously happy disposition HP:0100024
img Impulsivity HP:0100710
img Shyness HP:0100962
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Behavioural/Psychiatric Abnormality HP:0000708
img All HP:0000001img Phenotypic abnormality HP:00001185img Behavioural/Psychiatric Abnormality HP:0000708
Genes (377)

Species:
human : 377
Page Size
Current 25
  Page 1 of 16
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUP16P11.2100909384
img HP RolledUp, OMIM ID: 614671
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanDEL7Q11.23100653380
img HP RolledUp, OMIM ID: 613729
HumanDUP17Q21.31100529226
img HP RolledUp, OMIM ID: 613533
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanDUP16P13.3100505393
img HP RolledUp, OMIM ID: 613458
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanGRD1100312954Graves disease, susceptiblity to, 1
img HP RolledUp, OMIM ID: 275000
HumanDUPXP11.23P11.22100310754
img HP RolledUp, OMIM ID: 300801
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP RolledUp, OMIM ID: 612582
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDUP22Q11.2100240738
img HP RolledUp, OMIM ID: 608363
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDUP1Q21100217371Chromosome 1q21.1 duplication syndrome
img HP RolledUp, OMIM ID: 612475
HumanDEL1Q21100217370Chromosome 1q21.1 deletion syndrome
img HP RolledUp, OMIM ID: 612474
HumanJAWAD100192306Microcephaly with digital anomalies
img HP RolledUp, OMIM ID: 251255
HumanDEL2Q32Q33100190983Chromosome 2q32-q33 deletion syndrome
img HP RolledUp, OMIM ID: 612313
HumanMICRODEL15Q13.3100188869
img HP RolledUp, OMIM ID: 612001
HumanAUTS1100188832Autism, susceptibility to, 1
img HP RolledUp, OMIM ID: 209850
HumanMICRODEL3Q29100188788Chromosome 3q29 microdeletion syndrome
img HP RolledUp, OMIM ID: 609425
HumanAUTS14100187724autism, susceptibility to, 14
img HP RolledUp, OMIM ID: 611913
HumanCD24100133941CD24 molecule
img HP RolledUp, OMIM ID: 126200
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100851Abnormal emotion/affect behavior0self