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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: all > Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Genetic Diseases, Inborn [MESH:D030342] > Heredodegenerative Disorders, Nervous System [MESH:D020271] > Optic Atrophies, Hereditary [MESH:D015418] > Optic atrophy polyneuropathy deafness [MESH:C537129]

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31 results
Group by: C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Sort by: MeSH_UID, MeSH_NAME
 
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006632
 arsenic trioxide
C006632
 
  
  
  
MESH:C008261
 lead acetate
C008261
 
  
  
  
MESH:C015559
 trimellitic anhydride
C015559
 
  
  
  
MESH:C049325
 1,2-dithiol-3-thione
C049325
 
  
  
  
MESH:C061133
 tamibarotene
C061133
 
  
  
  
MESH:C089032
 rimonabant
C089032
 
  
  
  
MESH:C111118
 2',3,3',4',5-pentachloro-4-hydroxybiphenyl
C111118
 
  
  
  
MESH:C475919
 hydroxytamoxifen
C475919
 
  
  
  
MESH:C537129
 Optic atrophy polyneuropathy deafness
C537129
 
  
  
  
MESH:D000082
 Acetaminophen
D000082
 
  
  
  
MESH:D000643
 Ammonium Chloride
D000643
 
  
  
  
MESH:D001151
 Arsenic
D001151
 
  
  
  
MESH:D001564
 Benzo(a)pyrene
D001564
 
  
  
  
MESH:D002994
 Clofibrate
D002994
 
  
  
  
MESH:D003993
 Dibutyl Phthalate
D003993
 
  
  
  
MESH:D004041
 Dietary Fats
D004041
 
  
  
  
MESH:D004958
 Estradiol
D004958
 
  
  
  
MESH:D004997
 Ethinyl Estradiol
D004997
 
  
  
  
MESH:D005472
 Fluorouracil
D005472
 
  
  
  
MESH:D008748
 Methylcholanthrene
D008748
 
  
  
  
MESH:D010634
 Phenobarbital
D010634
 
  
  
  
MESH:D010894
 Piroxicam
D010894
 
  
  
  
MESH:D011374
 Progesterone
D011374
 
  
  
  
MESH:D013629
 Tamoxifen
D013629
 
  
  
  
MESH:D013749
 Tetrachlorodibenzodioxin
D013749
 
  
  
  
MESH:D013759
 Dronabinol
D013759
 
  
  
  
MESH:D014212
 Tretinoin
D014212
 
  
  
  
MESH:D014635
 Valproic Acid
D014635
 
  
  
  
MESH:D016572
 Cyclosporine
D016572
 
  
  
  
MESH:D016604
 Aflatoxin B1
D016604