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(e.g. Autoimmunity, Trichostatin A, rs6983267, DRD2, Apoptosis, Pseudomonas infection)
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QuickView for hemophilia B (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. F9
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. Coagulation factor IX
  2. Peptidase S1A, coagulation factor VII/IX/X/C/Z
  3. REACTOME_GAMMA_CARBOXYLATION_TRANSPORT_AND_AMINO_TERMINAL_CLEAVAGE_OF_PROTEINS
  4. Coagulation factor-like, Gla domain superfamily
  5. WU_APOPTOSIS_BY_CDKN1A_NOT_VIA_TP53
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Curated Studies

Most Correlated Studies

  1. Mouse Phenotypes - Hemophilia
  2. OMIM - Hereditary disorder by system
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Literature

Most Relevant Literature

  1. Molecular pathogenesis of a novel Met394Thr variant causing hemophilia B.
  2. Comprehensive analysis and prediction of long-term durability of factor IX activity following etrana…
  3. Molecular therapeutics of hemophilia A and B.
  4. Evaluation of treatment and outcome for patients with haemophilia A and haemophilia B on extended ha…
  5. Fitusiran prophylaxis in people with severe haemophilia A or haemophilia B without inhibitors (ATLAS…
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Clinical Trials

Most Relevant Clinical Trials

  1. A Gene Therapy Study for Hemophilia B
  2. Gene Therapy for Chinese Hemophilia B
  3. Socialization of Adult Men With Congenital Hemophilia A or B
  4. Needs Assessment of Knowledge, Beliefs, and Attitudes of Patients With Hemophilia B About Gene Thera…
  5. Females With Severe or Moderate Hemophilia A or B: A Multi-Center Study
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