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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: all > Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Musculoskeletal Abnormalities [MESH:D009139] > Craniofacial Abnormalities [MESH:D019465] > Maxillofacial Abnormalities [MESH:D019767]

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C05. Musculoskeletal Diseases: Musculoskeletal Diseases [MESH:D009140]
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1448 items, grouped by C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities (view ungrouped items)

Abruzzo Erickson syndrome [MESH:C535559] (1)   
MESH:C535559
 Abruzzo Erickson syndrome
C535559
 
  
  
  

Ackerman syndrome [MESH:C538170] (1)   
MESH:C538170
 Ackerman syndrome
C538170
 
  
  
  

Bifid Nose, Autosomal Dominant [MESH:C567781] (1)   
MESH:C567781
 Bifid Nose, Autosomal Dominant
C567781
 
  
  
  

Cherubism [MESH:D002636] (25)   
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C009505
 4,4'-diaminodiphenylmethane
C009505
 
  
  
  
MESH:C013038
 hydroxyhydroquinone
C013038
 
  
  
  
MESH:C016403
 2,4-dinitrotoluene
C016403
 
  
  
  
MESH:C028007
 nickel monoxide
C028007
 
  
  
  
all 25 items...

Dentofacial Deformities [MESH:D063169] (1)   
MESH:D063169
 Dentofacial Deformities
D063169
 
  
  
  

Jaw Abnormalities [MESH:D007569] (1435)   
MESH:C000516
 2-(2-cresyl)-4H-1-3-2-benzodioxaphosphorin-2-oxide
C000516
 
  
  
  
MESH:C000541
 cyclopamine
C000541
 
  
  
  
MESH:C000912
 diazoxon
C000912
 
  
  
  
MESH:C001277
 geldanamycin
C001277
 
  
  
  
MESH:C001803
 tempol
C001803
 
  
  
  
MESH:C002302
 dimethoxon
C002302
 
  
  
  
all 1435 items...

Maxillofacial Dysostosis [MESH:C563599] (1)   
MESH:C563599
 Maxillofacial Dysostosis
C563599
 
  
  
  

Maxillonasal dysplasia, Binder type [MESH:C536036] (1)   
MESH:C536036
 Maxillonasal dysplasia, Binder type
C536036
 
  
  
  

Oculomaxillofacial dysostosis [MESH:C537736] (1)   
MESH:C537736
 Oculomaxillofacial dysostosis
C537736
 
  
  
  

Robinow syndrome, autosomal recessive [MESH:C535863] (10)   
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C016517
 indole-3-carbinol
C016517
 
  
  
  
MESH:C027373
 potassium chromate(VI)
C027373
 
  
  
  
MESH:C045651
 epigallocatechin gallate
C045651
 
  
  
  
MESH:C535863
 Robinow syndrome, autosomal recessive
C535863
 
  
  
  
MESH:C547126
 AZM551248
C547126
 
  
  
  
all 10 items...

 (others) (2)   
MESH:D005050
 Etretinate
D005050
 
  
  
  
MESH:D019767
 Maxillofacial Abnormalities
D019767