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31 Possible Causes for 61A C, ANHAPTOGLOBINEMIA

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  • Immune Hemolytic Anemia

    Laboratory and clinical findings of severe hemolysis were present, including anhaptoglobinemia, microspherocytosis, splenomegaly, and transfusion dependence.[journals.lww.com]

    Missing: 61A C
  • Transfusion Reaction

    Anhaptoglobinemia, a condition that has high incidence in Asia, can cause allergic transfusion reactions or anaphylaxis in severe cases.[ncbi.nlm.nih.gov] We examined her genetic phenotype and detected anhaptoglobinemia, which occurs because of an allelic deletion in the Hp gene cluster.[ncbi.nlm.nih.gov] Here, we report the first case of anhaptoglobinemia causing anaphylactic transfusion reaction in Korea. KEYWORDS: Anaphylaxis; Haptoglobin; Platelet transfusion[ncbi.nlm.nih.gov]

    Missing: 61A C
  • Tacrolimus

    In conclusion, CYP3A5*3 is a major, and ABCB1 61A G is a novel, although minor, genetic factor affecting TAC C 0 /D in kidney transplant recipients. 2018 Nordic Association[ncbi.nlm.nih.gov] SNPs on TAC C 0 /D.[ncbi.nlm.nih.gov] This study aimed to investigate the effects of ABCB1 (61A G, 1199G A, 1236C T, 2677G T and 3435C T), CYP3A4*22, CYP3A5*3, NR1I2 (8055C T, 63396C T and -25385C T) and POR*28[ncbi.nlm.nih.gov]

    Missing: ANHAPTOGLOBINEMIA
  • Familial X-Linked Thrombocytosis

    […] are of genetic origin: Anemia, neonatal hemolytic Anemia, sideroblastic, pyridoxine-refractory Anemia, sideroblastic, with ataxia Anemia, sideroblastic Anemia, X-linked Anhaptoglobinemia[qlinics.com]

    Missing: 61A C
  • Primary Immune Deficiency Disorder

    DOCK8 Chr9:368196 c.1797 61A C NM_203447.3 rs786205596 DOCK8 Chr9:271626 c.54-1G T NM_203447.3 rs192864327 DOCK8 Chr9:317028 c.742-15T G NM_203447.3 rs111627162 DOCK8 Chr9[blueprintgenetics.com] .-141C G NM_001363.3 DKC1 ChrX:153991099 c.-142C G NM_001363.3 rs199422241 DKC1 ChrX:153993704 c.85-15T C NM_001363.3 DNMT3B Chr20:31395557 c.2421-11G A NM_006892.3 rs547940069[blueprintgenetics.com]

    Missing: ANHAPTOGLOBINEMIA
  • Primary CD59 Deficiency

    DOCK8 Chr9:368196 c.1797 61A C NM_203447.3 rs786205596 DOCK8 Chr9:271626 c.54-1G T NM_203447.3 rs192864327 DOCK8 Chr9:317028 c.742-15T G NM_203447.3 rs111627162 DOCK8 Chr9[blueprintgenetics.com] .-141C G NM_001363.3 DKC1 ChrX:153991099 c.-142C G NM_001363.3 rs199422241 DKC1 ChrX:153993704 c.85-15T C NM_001363.3 DNMT3B Chr20:31395557 c.2421-11G A NM_006892.3 rs547940069[blueprintgenetics.com]

    Missing: ANHAPTOGLOBINEMIA
  • Gallbladder Carcinoma

    C; rs13181); MSH2 (IVS1 9G C; rs2303426) and (-118T C; rs2303425); OGG1 Ser326Cys (Ex6-315C G; rs1052133) and (IVS4-15C G; rs2072668); XRCC1 Arg194Trp (Ex6-22C T; rs1799782[journals.plos.org] […] extended our previous work by jointly investigating 16 SNP genotypes in 8 genes belonging to DNA repair pathway [ ERCC2 Asp312Asn (Ex10-16G A; rs1799793) and Lys751Gln (Ex23 61A[journals.plos.org]

    Missing: ANHAPTOGLOBINEMIA
  • Immunodeficiency due to a Late Complement Component Deficiency

    DOCK8 Chr9:368196 c.1797 61A C NM_203447.3 rs786205596 DOCK8 Chr9:271626 c.54-1G T NM_203447.3 rs192864327 DOCK8 Chr9:317028 c.742-15T G NM_203447.3 rs111627162 DOCK8 Chr9[blueprintgenetics.com] .-141C G NM_001363.3 DKC1 ChrX:153991099 c.-142C G NM_001363.3 rs199422241 DKC1 ChrX:153993704 c.85-15T C NM_001363.3 DNMT3B Chr20:31395557 c.2421-11G A NM_006892.3 rs547940069[blueprintgenetics.com]

    Missing: ANHAPTOGLOBINEMIA
  • Familial Isolated Arrhythmogenic Right Ventricular Dysplasia Type 11

    611773 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps; OMIM:106180 Angiotensin I-Converting Enzyme; ACE OMIM:106150 Angiotensinogen; AGT OMIM:614081 Anhaptoglobinemia[informatics.jax.org]

    Missing: 61A C
  • Anonychia with Flexural Pigmentation

    611773 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps; OMIM:106180 Angiotensin I-Converting Enzyme; ACE OMIM:106150 Angiotensinogen; AGT OMIM:614081 Anhaptoglobinemia[informatics.jax.org]

    Missing: 61A C

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