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Details
Link-It Detail - Human Phenotype - Abnormal eating behavior
Debug Stats
  • ### Total Build Time: 25 ms 27.197 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 199 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=4 ms Completed: 4 ms rowSize= 456 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.333 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.107 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 21.954 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal eating behavior HP:0100738
Parents (1)
img Behavioural/Psychiatric Abnormality HP:0000708
Children (4)
img Pica HP:0011856
img Bulimia HP:0100739
img Hyperphagia HP:0000724
img Polyphagia HP:0002591
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 (45)

Species:
human : 45
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDEL2Q23.1100820633
img HP TAS, OMIM ID: 156200
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP TAS, OMIM ID: 606407
HumanGRD1100312954Graves disease, susceptiblity to, 1
img HP RolledUp, OMIM ID: 275000
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP TAS, OMIM ID: 607872
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanBULN337893Bulimia nervosa, susceptibility to
img HP RolledUp, OMIM ID: 607499
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP RolledUp, OMIM ID: 176270
HumanGRDX117189Graves disease, susceptibility to, X-linked
img HP RolledUp, OMIM ID: 275000
HumanIFIH164135interferon induced with helicase C domain 1
img HP RolledUp, OMIM ID: 275000
HumanMBD555777methyl-CpG binding domain protein 5
img HP TAS, OMIM ID: 156200
HumanMAGEL254551MAGE-like 2
img HP RolledUp, OMIM ID: 176270
HumanGRD250976Graves disease, susceptibility to, 2
img HP RolledUp, OMIM ID: 275000
HumanFOXP350943forkhead box P3
img HP RolledUp, OMIM ID: 222100
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
img HP RolledUp, OMIM ID: 269700
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
img HP RolledUp, OMIM ID: 222100
HumanNPAP123742nuclear pore associated protein 1
img HP RolledUp, OMIM ID: 176270
HumanAGPAT2105551-acylglycerol-3-phosphate O-acyltransferase 2
img HP RolledUp, OMIM ID: 608594
HumanMKRN3-AS110108
img HP RolledUp, OMIM ID: 176270
HumanSH2B310019SH2B adaptor protein 3
img HP RolledUp, OMIM ID: 222100
HumanPREPL9581prolyl endopeptidase-like
img HP TAS, OMIM ID: 606407
HumanHERC28924HECT and RLD domain containing E3 ubiquitin protein ligase 2
img HP RolledUp, OMIM ID: 176270
HumanMKRN37681makorin ring finger protein 3
img HP RolledUp, OMIM ID: 176270
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100738Abnormal eating behavior0self