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Results 1 - 10 of 11 for Congenital factor V deficiency
  1. Factor V deficiency 
    ... s disease Parahemophilia Proaccelerin deficiency Genetic Testing Registry: Congenital factor V deficiency Congenital factor V deficiency National Organization for Rare ...
    https://medlineplus.gov/genetics/condition/factor-v-deficiency - Genetics
  2. Factor XIII deficiency 
    ... Testing Registry: Factor XIII, A subunit, deficiency of Congenital factor XIII deficiency ... Biswas A, Ivaskevicius V, Thomas A, Oldenburg J. Coagulation factor XIII deficiency. ...
    https://medlineplus.gov/genetics/condition/factor-xiii-deficiency - Genetics
  3. Combined pituitary hormone deficiency 
    ... single disorder. Combined pituitary hormone deficiency can be congenital or acquired. Acquired combined pituitary hormone deficiency is caused by factors that occur later in life, such as infections ...
    https://medlineplus.gov/.../combined-pituitary-hormone-deficiency - Genetics
  4. Congenital leptin deficiency 
    ... be altered in congenital leptin deficiency are unknown.Congenital leptin deficiency is a rare cause of obesity. Researchers are studying the factors involved in more common forms of obesity. LEP ...
    https://medlineplus.gov/.../condition/congenital-leptin-deficiency - Genetics
  5. X-linked sideroblastic anemia 
    ... 10.1007/BF02110031. Citation on PubMed Bottomley SS. Congenital ... as a predisposing factor for late-onset X-linked sideroblastic anemia in ...
    https://medlineplus.gov/.../condition/x-linked-sideroblastic-anemia - Genetics
  6. COG5-congenital disorder of glycosylation 
    ... Kleinert P, Schnabel S, Baumgartner M, Hennet T. Deficiency in COG5 causes a ... Rymen D, Keldermans L, Race V, Regal L, Deconinck N, Dionisi-Vici C, Fung ...
    https://medlineplus.gov/...cog5-congenital-disorder-of-glycosylation - Genetics
  7. Laron syndrome 
    ... on PubMed Shevah O, Laron Z. Patients with congenital deficiency of ... of insulin-like growth factor deficiency. Endocr Dev. 2012;23:30-41. doi: ...
    https://medlineplus.gov/genetics/condition/laron-syndrome - Genetics
  8. Congenital hypothyroidism 
    ... CH CHT Congenital myxedema Cretinism Genetic Testing Registry: Congenital hypothyroidism Genetic Testing Registry: Deficiency of iodide peroxidase Genetic Testing Registry: Hypothyroidism due ...
    https://medlineplus.gov/genetics/condition/congenital-hypothyroidism - Genetics
  9. Trichothiodystrophy 
    ... Jun 13. Citation on PubMed Kleijer WJ, Laugel V, Berneburg M, Nardo T, Fawcett H, Gratchev A, Jaspers NG, Sarasin A, Stefanini M, Lehmann AR. Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome ...
    https://medlineplus.gov/genetics/condition/trichothiodystrophy - Genetics
  10. Kallmann syndrome 
    ... JP, Juul A, Maghnie M, Pitteloud N, Prevot V, Raivio T, Tena-Sempere M, Quinton R, Young J. Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment. Nat Rev ...
    https://medlineplus.gov/genetics/condition/kallmann-syndrome - Genetics
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