List of diseases (0-9)
From Self-sufficiency
The List of diseases starting with a non-letter is part of the complete list of diseases.
Diseases |
- 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, rare (NIH)
- 3-M syndrome, rare (NIH)
- 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
References
- ↑ 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