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Details
Link-It Detail - Human Phenotype - Abnormality of immune system physiology
Debug Stats
  • ### Total Build Time: 70 ms 27.389 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 214 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 213 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
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 453 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.662 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.168 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=50 ms Completed: 50 ms rowSize= 21.521 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.033 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of immune system physiology HP:0010978
Definition (1)
A functional abnormality of the `immune system` (FMA:9825).
Parents (1)
img Abnormality of the immune system HP:0002715
Children (8)
img Sepsis HP:0100806
img Abnormality of immune serum protein physiology HP:0011111
img Immunodeficiency HP:0002721
img Recurrent infections HP:0002719
img Abnormality of humoral immunity HP:0005368
img Immune dysregulation HP:0002958
img Autoimmunity HP:0002960
img Immunologic hypersensitivity HP:0100326
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the immune system HP:0002715
Genes (558)

Species:
human : 558
Page Size
Current 25
  Page 1 of 23
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPDA1100996949Patent ductus arteriosus, susceptibility to
img HP RolledUp, OMIM ID: 607411
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanCATMANS100862706Catel-Manzke syndrome
HumanMRXSCS100820761Mental retardation, X-linked, syndromic, Chudley-Schwartz type
img HP RolledUp, OMIM ID: 300861
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP TAS, OMIM ID: 252270
HumanMMRFCGU100529147Microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations
img HP RolledUp, OMIM ID: 613680
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP TAS, OMIM ID: 613406
HumanATPLS100499532antiphospholipid syndrome, familial
img HP RolledUp, OMIM ID: 107320
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanIBD25100270799Inflammatory bowel disease-25
img HP RolledUp, OMIM ID: 612567
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDUP22Q11.2100240738
img HP TAS, OMIM ID: 608363
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP TAS, OMIM ID: 607872
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP RolledUp, OMIM ID: 610543
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
HumanWM1100188787Macroglobulinemia, Waldenstrom, susceptibility to, 1
HumanDIP100188011interstitial pneumonitis, desquamative, familial
HumanAA1100034700Alopecia areata 1
img HP RolledUp, OMIM ID: 104000
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
HumanNKCD780917Natural killer cell deficiency, familial isolated
img HP RolledUp, OMIM ID: 609981
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010978Abnormality of immune system physiology0self