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Details
Link-It Detail - Human Phenotype - Abnormal neutrophil cell number
Debug Stats
  • ### Total Build Time: 72 ms 27.218 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 206 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=10 ms Completed: 10 ms rowSize= 447 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 750 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=22 ms Completed: 22 ms rowSize= 3.019 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=29 ms Completed: 29 ms rowSize= 21.659 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.025 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal neutrophil cell number HP:0011991
Parents (1)
img Abnormality of neutrophils HP:0001874
Children (2)
img Neutrophillia HP:0011897
img Neutropenia HP:0001875
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of neutrophils HP:0001874
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of neutrophils HP:0001874
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of neutrophils HP:0001874
Genes (59)

Species:
human : 59
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
img HP RolledUp, OMIM ID: 251110
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
img HP RolledUp, OMIM ID: 251100
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanDBA2114086Diamond-Blackfan anemia 2
img HP RolledUp, OMIM ID: 105650
HumanSLC46A1113235solute carrier family 46 (folate transporter), member 1
img HP RolledUp, OMIM ID: 229050
HumanG6PC392579glucose 6 phosphatase, catalytic, 3
img HP RolledUp, OMIM ID: 612541
HumanUSB179650U6 snRNA biogenesis 1
img HP RolledUp, OMIM ID: 604173
HumanLRRC8A56262leucine rich repeat containing 8 family, member A
img HP RolledUp, OMIM ID: 601495
HumanLMBRD155788LMBR1 domain containing 1
img HP RolledUp, OMIM ID: 277380
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img HP RolledUp, OMIM ID: 260400
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
img HP RolledUp, OMIM ID: 242900
HumanICOS29851inducible T-cell co-stimulator
HumanBLNK29760B-cell linker
img HP RolledUp, OMIM ID: 613502
HumanLAMTOR228956late endosomal/lysosomal adaptor, MAPK and MTOR activator 2
img HP RolledUp, OMIM ID: 610798
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
img HP RolledUp, OMIM ID: 277400
HumanSLC35A110559solute carrier family 35 (CMP-sialic acid transporter), member A1
img HP RolledUp, OMIM ID: 603585
HumanHAX110456HCLS1 associated protein X-1
img HP RolledUp, OMIM ID: 610738
HumanSTX118676syntaxin 11
img HP RolledUp, OMIM ID: 603552
HumanRFXANK8625regulatory factor X-associated ankyrin-containing protein
img HP RolledUp, OMIM ID: 209920
HumanAP3B18546adaptor-related protein complex 3, beta 1 subunit
img HP RolledUp, OMIM ID: 608233
HumanCXCR47852chemokine (C-X-C motif) receptor 4
img HP RolledUp, OMIM ID: 193670
HumanWAS7454Wiskott-Aldrich syndrome
HumanTCN26948transcobalamin II
img HP RolledUp, OMIM ID: 275350
HumanTAZ6901tafazzin
img HP RolledUp, OMIM ID: 302060
HumanSTK46789serine/threonine kinase 4
img HP RolledUp, OMIM ID: 614868
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011991Abnormal neutrophil cell number0self