List of diseases starting with a non-letter

From Wikipedia

The List of diseases starting with a non-letter is part of the complete list of diseases.

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

  • 11 beta hydroxylase deficiency
  • 10q Partial trisomy, rare (NIH) [1]
  • 11 beta hydroxysteroid dehydrogenase type 2 deficiency
  • 17 alpha hydroxylase deficiency
  • 17 beta hydroxysteroide dehydrogenase deficiency
  • 17 Beta-hydroxysteroid dehydrogenase deficiency, rare (NIH)
  • 18-Hydroxylase deficiency, rare (NIH)
  • 18p syndrome, rare (NIH)
  • 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
  • 3C syndrome, rare (NIH)
  • 3m syndrome
  • 3M syndrome, rare (NIH)
  • 4 alpha hydroxyphenylpyruvate hydroxylase deficiency
  • 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, rare (NIH)
  • 4-hydroxyphenylacetic aciduria, rare (NIH), Optic atrophy, [1]
  • 46 xx gonadal dysgenesis epibulbar dermoid
  • 46,XX Gonadal dysgenesis epibulbar dermoid, rare (NIH)
  • 47 XXY syndrome
  • 47 xyy syndrome
  • 47 XYY syndrome, rare (NIH), see Klinefelter's syndrome
  • 47,XXX syndrome, rare (NIH) , see Klinefelter's syndrome
  • 48 xxxx syndrome
  • 48 xxyy syndrome
  • 49 xxxxx syndrome
  • 49 xxxxy syndrome
  • 49,XXXXX syndrome, rare (NIH) , see Klinefelter's syndrome
  • 49,XXXXY syndrome, rare (NIH) , see Klinefelter's syndrome
  • 5 alpha reductase 2 deficiency
  • 5-alpha-Oxoprolinase deficiency, rare (NIH)
  • 5-Nucleotidase syndrome, rare (NIH)
  • 5q-syndrome, rare (NIH)
  • 6 alpha mercaptopurine sensitivity, rare (NIH)
  • 6-pyruvoyl-tetrahydropterin synthase deficiency, rare (NIH)
  • 6-pyruvoyltetrahydropterin synthase deficiency
  • 7-dehydrocholesterol reductase deficiency

[سمادول] References

  1. A rare disease (occurrence fewer than 1 case for 200,000) according to the public domain Rare Diseases Terms of the United States National Institute of Health