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Results 1 - 10 of 24 for Congenital gastrointestinal disorder
  1. ALG6-congenital disorder of glycosylation 
    ... H, Huijmans J, den Hollander J, Sinaasappel M. Gastrointestinal and other clinical manifestations in 17 children with congenital disorders of glycosylation type Ia, Ib, and Ic. J ...
    https://medlineplus.gov/...alg6-congenital-disorder-of-glycosylation - Genetics
  2. Alveolar capillary dysplasia with misalignment of pulmonary veins 
    ... Congenital alveolar capillary dysplasia National Organization for Rare Disorders (NORD) ... M, Kiely E, Spitz L, Malone M. Congenital alveolar capillary dysplasia and associated gastrointestinal anomalies. Fetal Pediatr Pathol. 2006 May-Jun;25( ...
    https://medlineplus.gov/...asia-with-misalignment-of-pulmonary-veins - Genetics
  3. Congenital hepatic fibrosis 
    Congenital hepatic fibrosis is a disease of the liver that is present from birth. The liver has ...
    https://medlineplus.gov/.../condition/congenital-hepatic-fibrosis - Genetics
  4. PGM3-congenital disorder of glycosylation 
    PGM3-congenital disorder of glycosylation (PGM3-CDG) is an inherited condition that primarily affects the immune system but can also involve other areas of ...
    https://medlineplus.gov/...pgm3-congenital-disorder-of-glycosylation - Genetics
  5. Congenital plasminogen deficiency 
    Congenital plasminogen deficiency is a disorder that results in inflamed growths on the mucous membranes, which are ...
    https://medlineplus.gov/.../congenital-plasminogen-deficiency - Genetics
  6. ALG1-congenital disorder of glycosylation 
    ALG1-congenital disorder of glycosylation (ALG1-CDG, also known as congenital disorder of glycosylation type Ik) is an inherited ... Carbohydrate deficient glycoprotein syndrome type Ik CDG1K CDGIk Congenital disorder of glycosylation type 1K Mannosyltransferase 1 deficiency ...
    https://medlineplus.gov/...alg1-congenital-disorder-of-glycosylation - Genetics
  7. Factor X deficiency 
    ... inherited form of factor X deficiency, known as congenital factor X deficiency, is caused by mutations in ... factor X deficiency, is more common than the congenital form. Acquired factor X deficiency can be caused ...
    https://medlineplus.gov/genetics/condition/factor-x-deficiency - Genetics
  8. Factor V deficiency 
    ... s disease Parahemophilia Proaccelerin deficiency Genetic Testing Registry: Congenital factor V deficiency Congenital factor V deficiency National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/factor-v-deficiency - Genetics
  9. Rothmund-Thomson syndrome 
    ... not show signs and symptoms of the condition. Congenital poikiloderma Poikiloderma atrophicans and cataract Poikiloderma congenitale Poikiloderma ...
    https://medlineplus.gov/genetics/condition/rothmund-thomson-syndrome - Genetics
  10. Lactose intolerance 
    ... lactase has both genetic and non-genetic causes.Congenital lactase deficiency, also called congenital alactasia, is a disorder in which infants are ... break down much of the lactose in milk. Congenital lactase deficiency is a rare disorder, though its ...
    https://medlineplus.gov/genetics/condition/lactose-intolerance - Genetics
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