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Details
Link-It Detail - Human Phenotype - Abnormality of myeloid leukocytes
Debug Stats
  • ### Total Build Time: 367 ms 23.830 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 206 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=4 ms Completed: 4 ms rowSize= 446 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.402 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.088 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=355 ms Completed: 355 ms rowSize= 18.328 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of myeloid leukocytes HP:0010974
Definition (1)
An abnormality of `myeloid leukocytes` (CL:0000766).
Parents (1)
img Abnormality of leukocytes HP:0001881
Children (4)
img Abnormality of mast cells HP:0100494
img Abnormality of phagocytes HP:0010977
img Abnormality of granulocytes HP:0001911
img Abnormality of macrophages HP:0004311
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of leukocytes HP:0001881
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of leukocytes HP:0001881
Genes (112)

Species:
human : 112
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNCF1653361neutrophil cytosolic factor 1
img HP RolledUp, OMIM ID: 233700
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
HumanSUMF1285362sulfatase modifying factor 1
HumanUNC13D201294unc-13 homolog D (C. elegans)
img HP RolledUp, OMIM ID: 608898
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP RolledUp, OMIM ID: 607115
HumanDBA2114086Diamond-Blackfan anemia 2
HumanSLC46A1113235solute carrier family 46 (folate transporter), member 1
HumanG6PC392579glucose 6 phosphatase, catalytic, 3
HumanDOCK881704dedicator of cytokinesis 8
HumanUSB179650U6 snRNA biogenesis 1
img HP RolledUp, OMIM ID: 604173
HumanDCLRE1C64421DNA cross-link repair 1C
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img HP RolledUp, OMIM ID: 609464
HumanRFMN57788Roifman syndrome
HumanLRRC8A56262leucine rich repeat containing 8 family, member A
img HP RolledUp, OMIM ID: 601495
HumanLMBRD155788LMBR1 domain containing 1
HumanSLC35C155343solute carrier family 35 (GDP-fucose transporter), member C1
img HP RolledUp, OMIM ID: 266265
HumanIRAK451135interleukin-1 receptor-associated kinase 4
img HP RolledUp, OMIM ID: 607676
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
HumanICOS29851inducible T-cell co-stimulator
img HP RolledUp, OMIM ID: 607594
HumanBLNK29760B-cell linker
img HP RolledUp, OMIM ID: 613502
HumanLAMTOR228956late endosomal/lysosomal adaptor, MAPK and MTOR activator 2
img HP RolledUp, OMIM ID: 610798
HumanHPLH127259hemophagocytic lymphohistiocytosis 1
img HP RolledUp, OMIM ID: 267700
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010974Abnormality of myeloid leukocytes0self