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Details
Link-It Detail - Human Phenotype - Abnormality of B cell number
Debug Stats
  • ### Total Build Time: 19 ms 19.999 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 203 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 356 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=2 ms Completed: 2 ms rowSize= 443 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 768 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.007 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 14.097 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of B cell number HP:0010975
Definition (1)
A deviation from the normal count of `B cells` (CL:0000236), i.e., the cells that are formed in the bone marrow, migrate to the peripheral lymphatic system, and mature into plasma cells or memory cells.
Parents (1)
img Abnormality of B cells HP:0002846
Children (2)
img B lymphocytopenia HP:0010976
img Increase in B cell number HP:0005404
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of B cells HP:0002846
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of B cells HP:0002846
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of B cells HP:0002846
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
img HP RolledUp, OMIM ID: 240500
HumanDCLRE1C64421DNA cross-link repair 1C
img HP RolledUp, OMIM ID: 603554
HumanLRRC8A56262leucine rich repeat containing 8 family, member A
img HP RolledUp, OMIM ID: 601495
HumanICOS29851inducible T-cell co-stimulator
img HP RolledUp, OMIM ID: 607594
img HP RolledUp, OMIM ID: 240500
HumanTNFRSF13B23495tumor necrosis factor receptor superfamily, member 13B
img HP RolledUp, OMIM ID: 240500
HumanRAG25897recombination activating gene 2
img HP RolledUp, OMIM ID: 603554
img HP RolledUp, OMIM ID: 601457
img HP RolledUp, OMIM ID: 233650
HumanRAG15896recombination activating gene 1
img HP RolledUp, OMIM ID: 601457
img HP RolledUp, OMIM ID: 233650
img HP RolledUp, OMIM ID: 603554
HumanNBN4683nibrin
img HP RolledUp, OMIM ID: 251260
HumanIGLL13543immunoglobulin lambda-like polypeptide 1
img HP RolledUp, OMIM ID: 601495
HumanIGHM3507immunoglobulin heavy constant mu
img HP RolledUp, OMIM ID: 601495
HumanGFI12672growth factor independent 1 transcription repressor
img HP RolledUp, OMIM ID: 613107
HumanCR21380complement component (3d/Epstein Barr virus) receptor 2
img HP RolledUp, OMIM ID: 240500
HumanCD19930CD19 molecule
img HP RolledUp, OMIM ID: 240500
HumanCASP10843caspase 10, apoptosis-related cysteine peptidase
img HP RolledUp, OMIM ID: 603909
HumanADA100adenosine deaminase
img HP RolledUp, OMIM ID: 102700
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010975Abnormality of B cell number0self