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Results 1 - 10 of 14 for Hb SS disease
  1. Sickle cell disease 
    ... disorder due to hemoglobin S Genetic Testing Registry: Hb SS disease Sickle cell anemia National Organization for Rare Disorders (NORD) ClinicalTrials.gov SICKLE CELL DISEASE PubMed Ashley-Koch A, Yang Q, Olney RS. Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review. ...
    https://medlineplus.gov/genetics/condition/sickle-cell-disease - Genetics
  2. Omenn syndrome 
    ... Cunningham-Rundles C, Etzioni A, Franco JL, Gaspar HB, Holland SM, Klein C, Nonoyama S, Ochs HD, Oksenhendler E, Picard C, Puck JM, Sullivan K, Tang ML. Primary immunodeficiency diseases: an update on the classification from the international ...
    https://medlineplus.gov/genetics/condition/omenn-syndrome - Genetics
  3. Alpha thalassemia 
    ... 2; HBA2 ALPHA-THALASSEMIA PubMed ... available. Citation on PubMed Chui DH. Alpha-thalassemia: Hb H disease and Hb Barts hydrops fetalis. Ann ...
    https://medlineplus.gov/genetics/condition/alpha-thalassemia - Genetics
  4. Gaucher disease 
    ... Cerebroside lipidosis syndrome Gaucher splenomegaly Gaucher syndrome Gaucher's disease Gauchers disease GD Glucocerebrosidase deficiency Glucocerebrosidosis Glucosyl cerebroside ...
    https://medlineplus.gov/genetics/condition/gaucher-disease -
  5. Autoimmune lymphoproliferative syndrome 
    ... Y, Koike K, Kojima S, Takao A, Mizutani S. Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation. Blood. 2011 Mar 10; ... Citation on PubMed Worth A, Thrasher AJ, Gaspar HB. Autoimmune ... molecular basis of disease and clinical phenotype. Br J Haematol. 2006 Apr; ...
    https://medlineplus.gov/.../autoimmune-lymphoproliferative-syndrome - Genetics
  6. Lung cancer 
    ... each cell is sufficient to increase a person's chance of developing the disease. It is important to note that people inherit ...
    https://medlineplus.gov/genetics/condition/lung-cancer - Genetics
  7. Bladder cancer 
    ... each cell is sufficient to increase a person's chance of developing the disease. It is important to note that people inherit ...
    https://medlineplus.gov/genetics/condition/bladder-cancer - Genetics
  8. Lissencephaly with cerebellar hypoplasia 
    ... A, Apse KA, Ozdel O, Atmaca M, Zencir S, Bagci H, Walsh CA. The role of RELN in lissencephaly and neuropsychiatric disease. Am J Med Genet B Neuropsychiatr Genet. 2007 ...
    https://medlineplus.gov/.../lissencephaly-with-cerebellar-hypoplasia - Genetics
  9. Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia 
    ... Wider C, Graff-Radford NR, Nelson PT, Clark HB, Wszolek ZK, Dickson DW, Knopman DS, Rademakers R. CSF1R mutations link POLD and HDLS as a single disease entity. Neurology. 2013 Mar 12;80(11):1033- ...
    https://medlineplus.gov/...-with-axonal-spheroids-and-pigmented-glia - Genetics
  10. Saul-Wilson syndrome 
    ... JB, Wegner J, Tiemeyer M, Aoki K; Undiagnosed Diseases Network; Scottish Genome Partnership; Nordgren A, Hammarsjo A, Duker AL, Rohena L, Hove HB, Ek J, Adams D, Tifft CJ, Onyekweli T, ...
    https://medlineplus.gov/genetics/condition/saul-wilson-syndrome - Genetics
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