List of diseases (0–9)

This is a list of diseases starting with a digit.

1–3
  • 11 beta hydroxylase deficiency
  • 10q partial trisomy
  • 11 beta hydroxysteroid dehydrogenase type 2 deficiency
  • 17 alpha hydroxylase deficiency
  • 17 beta hydroxysteroide dehydrogenase deficiency
  • 17-beta-hydroxysteroid dehydrogenase deficiency, rare (NIH)
  • 17q21.31 microdeletion syndrome
  • 18-Hydroxylase deficiency, rare (NIH)
  • 18p deletion syndrome
  • 1p36 deletion syndrome, rare (NIH)
  • 2-hydroxyethyl methacrylate sensitization, rare (NIH)
  • 2-hydroxyglutaricaciduria
  • 2-Hydroxyglutaricaciduria, rare (NIH)
  • 2-Methylacetoacetyl CoA thiolase deficiency, rare (NIH)
  • 2,8 dihydroxy-adenine urolithiasis
  • 21 hydroxylase deficiency
  • 22q11.2 deletion syndrome, rare (NIH)
  • 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency, rare (NIH)
  • 3 alpha methylcrotonyl-coa carboxylase 2 deficiency, rare (NIH)
  • 3 alpha methylglutaconic aciduria, type 3, rare (NIH)
  • 3 beta hydroxysteroid dehydrogenase deficiency
  • 3 hydroxyisobutyric aciduria
  • 3 methylcrotonic aciduria
  • 3 methylglutaconyl coa hydratase deficiency
  • 3-hydroxy 3-methyl glutaryl-coa lyase deficiency
  • 3-hydroxyacyl-coa dehydrogenase deficiency
  • 3 hydroxyisobutyric aciduria, rare (NIH)
  • 3-methyl crotonyl-coa carboxylase deficiency
  • 3-methyl glutaconic aciduria
  • 3C syndrome, rare (NIH)
  • 3-M syndrome, rare (NIH)
  • 3q29 microdeletion syndrome

4–9
  • 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, rare (NIH)
  • 4-hydroxyphenylacetic aciduria, rare (NIH), Optic atrophy,
  • 46 xx gonadal dysgenesis epibulbar dermoid, rare (NIH)
  • 47, XXY syndrome
  • 47, XYY syndrome
  • 47, XXX syndrome
  • 48, XXXX syndrome
  • 48, XXYY syndrome
  • 49, XXXXX syndrome
  • 49, XXXXY syndrome
  • 5 alpha reductase 2 deficiency
  • 5-alpha-Oxoprolinase deficiency, rare (NIH)
  • 5-Nucleotidase syndrome, rare (NIH)
  • 5p minus syndrome
  • 5q- syndrome
  • 6 alpha mercaptopurine sensitivity, rare (NIH)
  • 6-pyruvoyl-tetrahydropterin synthase deficiency, rare (NIH)
  • 6-pyruvoyltetrahydropterin synthase deficiency
  • 7-dehydrocholesterol reductase deficiency
  • 8p23.1 duplication syndrome
  • 9q34 deletion syndrome
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