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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 1 and deafness [MESH:C537124]

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30 results
Group by: C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Sort by: MeSH_UID, MeSH_NAME
 
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C009505
 4,4'-diaminodiphenylmethane
C009505
 
  
  
  
MESH:C023514
 2,6-dinitrotoluene
C023514
 
  
  
  
MESH:C025643
 vinclozolin
C025643
 
  
  
  
MESH:C055494
 caffeic acid phenethyl ester
C055494
 
  
  
  
MESH:C059514
 resveratrol
C059514
 
  
  
  
MESH:C089032
 rimonabant
C089032
 
  
  
  
MESH:C089730
 rosiglitazone
C089730
 
  
  
  
MESH:C496966
 Eudragit RSPO
C496966
 
  
  
  
MESH:C537124
 Optic atrophy 1 and deafness
C537124
 
  
  
  
MESH:D000082
 Acetaminophen
D000082
 
  
  
  
MESH:D000643
 Ammonium Chloride
D000643
 
  
  
  
MESH:D001564
 Benzo(a)pyrene
D001564
 
  
  
  
MESH:D003993
 Dibutyl Phthalate
D003993
 
  
  
  
MESH:D004041
 Dietary Fats
D004041
 
  
  
  
MESH:D004052
 Diethylnitrosamine
D004052
 
  
  
  
MESH:D004221
 Disulfiram
D004221
 
  
  
  
MESH:D004997
 Ethinyl Estradiol
D004997
 
  
  
  
MESH:D005419
 Flavonoids
D005419
 
  
  
  
MESH:D006830
 Hydralazine
D006830
 
  
  
  
MESH:D010894
 Piroxicam
D010894
 
  
  
  
MESH:D012402
 Rotenone
D012402
 
  
  
  
MESH:D012643
 Selenium
D012643
 
  
  
  
MESH:D013629
 Tamoxifen
D013629
 
  
  
  
MESH:D013749
 Tetrachlorodibenzodioxin
D013749
 
  
  
  
MESH:D013893
 Thiram
D013893
 
  
  
  
MESH:D014635
 Valproic Acid
D014635
 
  
  
  
MESH:D015215
 Zidovudine
D015215
 
  
  
  
MESH:D018817
 N-Methyl-3,4-methylenedioxyamphetamine
D018817
 
  
  
  
MESH:D019259
 Lamivudine
D019259