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Details
Link-It Detail - Human Phenotype - Abnormality of leukocytes
Debug Stats
  • ### Total Build Time: 43 ms 32.414 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 200 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 198 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=0 Completed: 0 ms rowSize= 808 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 4.658 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.121 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=31 ms Completed: 31 ms rowSize= 23.293 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of leukocytes HP:0001881
Definition (1)
An abnormality of `leukocytes` (CL:0000738).
Parents (2)
img Abnormality of blood and blood-forming tissues HP:0001871
img Abnormality of cellular immune system HP:0010987
Children (14)
img Neutrophil inclusion bodies HP:0008264
img Abnormality of myeloid leukocytes HP:0010974
img Abnormal leukocyte count HP:0011893
img Leukocyte inclusion bodies (Dohle-like bodies) HP:0001932
img Reduced lymphocyte surface expression of CD43 (sialophorin) HP:0001983
img Leukopenia HP:0001882
img Leukemia HP:0001909
img Cellular metachromasia HP:0003653
img Abnormality of granulocytes HP:0001911
img Reduced leukocyte alkaline phosphatase HP:0004852
img Elevated leukocyte alkaline phosphatase HP:0008318
img Abnormality of lymphocytes HP:0004332
img Leukocytosis HP:0001974
img Elevated intracellular cystine HP:0003358
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of blood and blood-forming tissues HP:0001871
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of cellular immune system HP:0010987
Genes (368)

Species:
human : 368
Page Size
Current 25
  Page 1 of 15
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMRXSCS100820761Mental retardation, X-linked, syndromic, Chudley-Schwartz type
img HP RolledUp, OMIM ID: 300861
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanALL1100310785Leukemia, acute lymphocytic, susceptibility to, 1
img HP RolledUp, OMIM ID: 613065
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
img HP RolledUp, OMIM ID: 152700
HumanWM1100188787Macroglobulinemia, Waldenstrom, susceptibility to, 1
img HP RolledUp, OMIM ID: 153600
HumanAA1100034700Alopecia areata 1
img HP RolledUp, OMIM ID: 104000
HumanNKCD780917Natural killer cell deficiency, familial isolated
img HP RolledUp, OMIM ID: 609981
HumanSFTPA2729238surfactant protein A2
img HP RolledUp, OMIM ID: 178500
HumanMUC5B727897mucin 5B, oligomeric mucus/gel-forming
img HP RolledUp, OMIM ID: 178500
HumanSFTPA1653509surfactant protein A1
img HP RolledUp, OMIM ID: 178500
HumanNCF1653361neutrophil cytosolic factor 1
img HP RolledUp, OMIM ID: 233700
HumanMPDMRS574047Martin-Probst deafness-mental retardation syndrome
img HP RolledUp, OMIM ID: 300519
HumanCLN9497231ceroid-lipofuscinosis, neuronal 9
img HP RolledUp, OMIM ID: 609055
HumanMIR16-1406950
img HP RolledUp, OMIM ID: 151400
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
img HP RolledUp, OMIM ID: 152700
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
img HP RolledUp, OMIM ID: 601675
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
img HP RolledUp, OMIM ID: 251110
HumanSUMF1285362sulfatase modifying factor 1
img HP RolledUp, OMIM ID: 272200
HumanPTRF284119polymerase I and transcript release factor
img HP RolledUp, OMIM ID: 613327
HumanRAB40AL282808RAB40A, member RAS oncogene family-like
img HP RolledUp, OMIM ID: 300519
HumanELMOD2255520ELMO/CED-12 domain containing 2
img HP RolledUp, OMIM ID: 178500
HumanUNC13D201294unc-13 homolog D (C. elegans)
img HP RolledUp, OMIM ID: 608898
HumanKLHDC8B200942kelch domain containing 8B
img HP RolledUp, OMIM ID: 236000
HumanSLEH1170682systemic lupus erythematosus with hemolytic anemia 1
img HP RolledUp, OMIM ID: 152700
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001881Abnormality of leukocytes0self