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Details
Link-It Detail - Human Phenotype - Abnormality of blood and blood-forming tissues
Debug Stats
  • ### Total Build Time: 73 ms 29.860 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 222 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_GENES gt=70 ms Completed: 70 ms rowSize= 22.029 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.041 KB
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  • Reload Stats
Human Phenotype (1)
Abnormality of blood and blood-forming tissues HP:0001871
Definition (1)
An abnormality of the `hematopoietic system` (FMA:9667).
Parents (1)
img Phenotypic abnormality HP:0000118
Children (14)
img Abnormality of coagulation HP:0001928
img Abnormal thrombosis HP:0001977
img Abnormality of erythroid lineage cell HP:0010973
img Abnormality of thrombocytes HP:0001872
img Abnormality of the kinin-kallikrein system HP:0005559
img Abnormality of leukocytes HP:0001881
img Abnormality of the spleen HP:0001743
img Extramedullary hematopoiesis HP:0001978
img Abnormality of erythrocytes HP:0001877
img Abnormality of bone marrow cell morphology HP:0005561
img Hematological neoplasm HP:0004377
img Pancytopenia HP:0001876
img Abnormal bleeding HP:0001892
img Abnormality of histiocytes HP:0004310
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001183img Phenotypic abnormality HP:0000118
Genes (929)

Species:
human : 929
Page Size
Current 25
  Page 1 of 38
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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
HumanMYMY4100653379Moyamoya disease 4
HumanFWS100529224Forsythe-Wakeling syndrome
img HP RolledUp, OMIM ID: 613606
HumanIBD11100529151Inflammatory bowel disease 11
HumanOCLN100506658occludin
img HP RolledUp, OMIM ID: 251290
HumanATPLS100499532antiphospholipid syndrome, familial
img HP RolledUp, OMIM ID: 107320
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
img HP RolledUp, OMIM ID: 300194
HumanALL1100310785Leukemia, acute lymphocytic, susceptibility to, 1
img HP RolledUp, OMIM ID: 613065
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
img HP RolledUp, OMIM ID: 613024
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP RolledUp, OMIM ID: 610543
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
img HP RolledUp, OMIM ID: 152700
HumanWM1100188787Macroglobulinemia, Waldenstrom, susceptibility to, 1
img HP RolledUp, OMIM ID: 153600
HumanTEC100124696transient erythroblastopenia of childhood
img HP RolledUp, OMIM ID: 227050
HumanAA1100034700Alopecia areata 1
img HP RolledUp, OMIM ID: 104000
HumanEDS8791254Ehlers-Danlos syndrome, type VIII
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP IEA, OMIM ID: 149000
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
HumanNKCD780917Natural killer cell deficiency, familial isolated
img HP RolledUp, OMIM ID: 609981
HumanAUNX1751798auditory neuropathy, X-linked recessive 1
img HP RolledUp, OMIM ID: 300614
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
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001871Abnormality of blood and blood-forming tissues0self