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Results 21 - 30 of 45 for Factor H deficiency
  1. Beta-ureidopropionase deficiency 
    ... gene mutation, along with other genetic and environmental factors, may determine whether people with beta-ureidopropionase deficiency develop neurological problems and the severity of these ...
    https://medlineplus.gov/.../beta-ureidopropionase-deficiency - Genetics
  2. Proopiomelanocortin deficiency 
    ... complex forms of obesity. Researchers are studying other factors that are likely involved in these forms. POMC POMC deficiency is inherited in an autosomal recessive pattern, which ...
    https://medlineplus.gov/.../condition/proopiomelanocortin-deficiency - Genetics
  3. Generalized pustular psoriasis 
    ... A, Casanova JL, Sims JE, Turki H, Bachelez H, Smahi A. Interleukin-36-receptor antagonist deficiency and generalized pustular psoriasis. N Engl J Med. ...
    https://medlineplus.gov/.../condition/generalized-pustular-psoriasis - Genetics
  4. Monoamine oxidase A deficiency 
    ... behavioral problems in people with monoamine oxidase A deficiency.Research suggests that environmental factors, such as mistreatment in childhood, may impact the ...
    https://medlineplus.gov/.../condition/monoamine-oxidase-a-deficiency - Genetics
  5. Spina bifida 
    ... vitamin folate (also called vitamin B9). A shortage (deficiency) of this vitamin is an established risk factor for neural tube defects like spina bifida. Changes ...
    https://medlineplus.gov/genetics/condition/spina-bifida - Genetics
  6. Congenital leptin deficiency 
    ... 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
  7. 3-methylglutaconyl-CoA hydratase deficiency 
    ... children, researchers speculate that other genes or environmental factors may play a role in the features of 3-methylglutaconyl-CoA hydratase deficiency. AUH This condition is inherited in an autosomal ...
    https://medlineplus.gov/...methylglutaconyl-coa-hydratase-deficiency - Genetics
  8. X-linked sideroblastic anemia 
    ... Citation on PubMed Nakajima O, Takahashi S, Harigae H, Furuyama K, Hayashi N, Sassa S, Yamamoto M. Heme deficiency in erythroid lineage causes differentiation arrest and cytoplasmic ...
    https://medlineplus.gov/.../condition/x-linked-sideroblastic-anemia - Genetics
  9. Trimethylaminuria 
    ... TRIMETHYLAMINURIA; TMAU PubMed Chalmers RA, Bain MD, Michelakakis H, Zschocke J, Iles RA. Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children. J Inherit Metab Dis. 2006 Feb; ...
    https://medlineplus.gov/genetics/condition/trimethylaminuria - Genetics
  10. Restless legs syndrome 
    ... results from a combination of genetic and environmental factors, many of which are unknown.Studies suggest that restless legs syndrome is related to a shortage (deficiency) of iron in certain parts of the brain. ...
    https://medlineplus.gov/genetics/condition/restless-legs-syndrome - Genetics
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