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Results 1 - 10 of 17 for Not genetically inherited
  1. Uromodulin-associated kidney disease 
    ... of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome. Kidney Int. 2006 Sep;70(6):1155-69. doi: 10.1038/sj.ki.5001728. Epub 2006 Aug 2. Citation on PubMed
    https://medlineplus.gov/.../uromodulin-associated-kidney-disease - Genetics
  2. 17-beta hydroxysteroid dehydrogenase 3 deficiency 
    ... in some affected individuals. ... signs and symptoms of the condition. Individuals who are genetically male and have two copies of a mutated ...
    https://medlineplus.gov/...hydroxysteroid-dehydrogenase-3-deficiency - Genetics
  3. 5-alpha reductase deficiency 
    ... sex characteristics during puberty. ... of the condition. Although people who are genetically female (with two X chromosomes in each cell) ...
    https://medlineplus.gov/.../condition/5-alpha-reductase-deficiency - Genetics
  4. Autoimmune lymphoproliferative syndrome 
    ... Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome. Blood. 2010 Jun 24; ...
    https://medlineplus.gov/.../autoimmune-lymphoproliferative-syndrome - Genetics
  5. Leydig cell hypoplasia 
    ... milder signs and symptoms. ... have mutations in both copies of the LHCGR gene and are genetically male (with one X and one Y chromosome ...
    https://medlineplus.gov/genetics/condition/leydig-cell-hypoplasia - Genetics
  6. Metachromatic leukodystrophy 
    ... worldwide. The condition is more common in certain genetically isolated populations: 1 in 75 in a small ... called pseudoarylsulfatase deficiency. ARSA PSAP This condition is inherited in an autosomal recessive pattern, which means both ...
    https://medlineplus.gov/.../condition/metachromatic-leukodystrophy - Genetics
  7. Sudden infant death with dysgenesis of the testes syndrome 
    ... and breathing problems.Infants with SIDDT who are genetically male, with one X chromosome and one Y ... or clearly female. In affected infants who are genetically female, with two X chromosomes in each cell, ...
    https://medlineplus.gov/...th-with-dysgenesis-of-the-testes-syndrome - Genetics
  8. Huntington's disease-like syndrome 
    ... SJ. Huntington's disease phenocopies are clinically and genetically heterogeneous. Mov Disord. 2008 Apr 15;23(5): ...
    https://medlineplus.gov/.../huntingtons-disease-like-syndrome - Genetics
  9. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation 
    ... and spinal cord involvement and high lactate: a genetically proven case with distinct MRI findings. J Neurol ...
    https://medlineplus.gov/...al-cord-involvement-and-lactate-elevation - Genetics
  10. Williams syndrome 
    ... VS, Morris CA, Berman KF. Neural correlates of genetically abnormal social cognition in Williams syndrome. Nat Neurosci. ...
    https://medlineplus.gov/genetics/condition/williams-syndrome - Genetics
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