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Details
Link-It Detail - Human Phenotype - Abnormality of multiple cell lineages in the bone marrow
Debug Stats
  • ### Total Build Time: 22 ms 27.189 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 231 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=2 ms Completed: 2 ms rowSize= 463 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.377 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.178 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 22.763 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.050 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of multiple cell lineages in the bone marrow HP:0012145
Parents (1)
img Abnormality of bone marrow cell morphology HP:0005561
Children (4)
img Megaloblastic bone marrow HP:0001980
img Pancytopenia HP:0001876
img Myelofibrosis HP:0011974
img Bone marrow hypocellularity HP:0005528
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of bone marrow cell morphology HP:0005561
Genes (70)

Species:
human : 70
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMPDMRS574047Martin-Probst deafness-mental retardation syndrome
img HP RolledUp, OMIM ID: 300519
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 613985
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
img HP RolledUp, OMIM ID: 251110
HumanRAB40AL282808RAB40A, member RAS oncogene family-like
img HP RolledUp, OMIM ID: 300519
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
img HP RolledUp, OMIM ID: 251100
HumanSLC46A1113235solute carrier family 46 (folate transporter), member 1
img HP RolledUp, OMIM ID: 229050
HumanBRIP183990BRCA1 interacting protein C-terminal helicase 1
img HP RolledUp, OMIM ID: 609054
HumanCTC180169CTS telomere maintenance complex component 1
img HP RolledUp, OMIM ID: 612199
HumanPALB279728partner and localizer of BRCA2
img HP RolledUp, OMIM ID: 610832
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img HP RolledUp, OMIM ID: 181000
HumanWDR1957728WD repeat domain 19
img HP RolledUp, OMIM ID: 614378
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
img HP RolledUp, OMIM ID: 607426
HumanCOQ957017coenzyme Q9 homolog (S. cerevisiae)
img HP RolledUp, OMIM ID: 607426
HumanADCK356997aarF domain containing kinase 3
img HP RolledUp, OMIM ID: 607426
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
img HP RolledUp, OMIM ID: 181000
HumanLMBRD155788LMBR1 domain containing 1
img HP RolledUp, OMIM ID: 277380
HumanNHP255651NHP2 ribonucleoprotein
img HP RolledUp, OMIM ID: 613987
img HP RolledUp, OMIM ID: 224230
HumanNOP1055505NOP10 ribonucleoprotein
img HP RolledUp, OMIM ID: 224230
HumanFANCI55215Fanconi anemia, complementation group I
img HP RolledUp, OMIM ID: 609053
HumanWRAP5355135WD repeat containing, antisense to TP53
img HP RolledUp, OMIM ID: 613988
HumanAPTX54840aprataxin
img HP RolledUp, OMIM ID: 607426
HumanRTEL151750regulator of telomere elongation helicase 1
img HP RolledUp, OMIM ID: 615190
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img HP RolledUp, OMIM ID: 260400
HumanOSTM128962osteopetrosis associated transmembrane protein 1
img HP RolledUp, OMIM ID: 259700
HumanCOQ227235coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
img HP RolledUp, OMIM ID: 607426
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012145Abnormality of multiple cell lineages in the bone marrow0self