List of diseases (0-9)

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

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*11 beta hydroxylase deficiency
*10q Partial trisomy, rare (NIH) A rare disease (occurrence fewer than 1 case for 200,000) according to the public domain [http://rarediseases.info.nih.gov/asp/diseases/diseases.asp Rare Diseases Terms] of the United States National Institute of Health]
*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, rare (NIH)
*4-hydroxyphenylacetic aciduria, rare (NIH), Optic atrophy, [http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=258501]
*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