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Results 41 - 50 of 53 for Inherited thrombocytopenia
  1. Fanconi anemia 
    ... clotting problems due to low numbers of platelets (thrombocytopenia). People with Fanconi anemia may also develop myelodysplastic ... RFWD3 SLX4 UBE2T XRCC2 Fanconi anemia is typically inherited in an autosomal recessive pattern, which means both ...
    https://medlineplus.gov/genetics/condition/fanconi-anemia - Genetics
  2. X chromosome 
    ... idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder. J ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  3. Blood Disorders (National Library of Medicine)  
    ... be acute or chronic. Many blood disorders are inherited. Other causes include other diseases, side effects of ...
    https://medlineplus.gov/blooddisorders.html - Health Topics
  4. Bruising and Bleeding (Merck & Co., Inc.)  
    Bleeding Disorders/Start Here ... Bleeding Disorders ... Merck & Co., Inc. ... Bruising and Bleeding - Learn about the causes, symptoms, diagnosis & treatment from the Merck ...
    https://www.merckmanuals.com/.../bruising-and-bleeding - External Health Links
  5. Hereditary folate malabsorption 
    ... In addition, some affected individuals have fewer platelets (thrombocytopenia), which means they can bruise easily. Without treatment, ... of hereditary folate malabsorption. SLC46A1 This condition is inherited in an autosomal recessive pattern, which means both ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  6. 1q21.1 microdeletion 
    ... distinguish it from the genetic change that causes thrombocytopenia-absent radius syndrome (TAR syndrome). TAR syndrome results ... GJA8 GPR89B HYDIN PRKAB2 1q21.1 microdeletion is inherited in an autosomal dominant pattern, which means that ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
  7. Gray platelet syndrome 
    ... phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and alpha-granule deficiency. Haematologica. 2013 Jun;98( ...
    https://medlineplus.gov/genetics/condition/gray-platelet-syndrome - Genetics
  8. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome 
    ... low levels of red blood cells (anemia), platelets (thrombocytopenia), or certain white blood cells (neutropenia) because these ... people with IPEX syndrome. FOXP3 IPEX syndrome is inherited in an X-linked recessive pattern. The FOXP3 ...
    https://medlineplus.gov/...ocrinopathy-enteropathy-x-linked-syndrome - Genetics
  9. Niemann-Pick disease 
    ... a low number of platelets in the blood (thrombocytopenia). They also have short stature and slowed mineralization ... and C2. NPC1 NPC2 SMPD1 This condition is inherited in an autosomal recessive pattern, which means both ...
    https://medlineplus.gov/genetics/condition/niemann-pick-disease - Genetics
  10. Core binding factor acute myeloid leukemia 
    ... and a reduction in the amount of platelets (thrombocytopenia) can result in easy bruising and abnormal bleeding. ... chromosome 21 chromosome 8 CBF-AML is not inherited but arises from genetic rearrangements in the body' ...
    https://medlineplus.gov/...ore-binding-factor-acute-myeloid-leukemia - Genetics
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