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C05. Musculoskeletal Diseases: all > Musculoskeletal Diseases [MESH:D009140] > Bone Diseases [MESH:D001847] > Bone Diseases, Metabolic [MESH:D001851] > Osteoporosis [MESH:D010024]

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3037 items, grouped by C05. Musculoskeletal Diseases (view ungrouped items)

Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis [MESH:C565960] (1)   
MESH:C565960
 Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis
C565960
 
  
  
  

Exudative vitreoretinopathy 1 [MESH:C536382] (34)   
MESH:C012589
 trichostatin A
C012589
 
  
  
  
MESH:C015559
 trimellitic anhydride
C015559
 
  
  
  
MESH:C018021
 cobaltous chloride
C018021
 
  
  
  
MESH:C023514
 2,6-dinitrotoluene
C023514
 
  
  
  
MESH:C061365
 flusilazole
C061365
 
  
  
  
MESH:C107676
 deguelin
C107676
 
  
  
  
all 34 items...

Female Athlete Triad Syndrome [MESH:D053716] (1)   
MESH:D053716
 Female Athlete Triad Syndrome
D053716
 
  
  
  

Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy [MESH:C564264] (1)   
MESH:C564264
 Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy
C564264
 
  
  
  

Hernandez Fragoso syndrome [MESH:C536062] (1)   
MESH:C536062
 Hernandez Fragoso syndrome
C536062
 
  
  
  

Juvenile osteoporosis [MESH:C537700] (2)   
MESH:C537700
 Juvenile osteoporosis
C537700
 
  
  
  
MESH:D004872
 Ergocalciferols
D004872
 
  
  
  

Macroepiphyseal dysplasia, McAlister Coe type [MESH:C537721] (1)   
MESH:C537721
 Macroepiphyseal dysplasia, McAlister Coe type
C537721
 
  
  
  

Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1 [MESH:C567363] (1)   
MESH:C567363
 Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1
C567363
 
  
  
  

Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2 [MESH:C567362] (1)   
MESH:C567362
 Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2
C567362
 
  
  
  

Neurologic Disease, Infantile Multisystem, with Osseous Fragility [MESH:C564954] (1)   
MESH:C564954
 Neurologic Disease, Infantile Multisystem, with Osseous Fragility
C564954
 
  
  
  

Osteoporosis, Postmenopausal [MESH:D015663] (2351)   
MESH:C000188
 alachlor
C000188
 
  
  
  
MESH:C000228
 aristolochic acid I
C000228
 
  
  
  
MESH:C000474
 cholestane-3,5,6-triol
C000474
 
  
  
  
MESH:C000488
 cladosporin
C000488
 
  
  
  
MESH:C000499
 ferric oxide
C000499
 
  
  
  
MESH:C000873
 methylprednisolone acetate
C000873
 
  
  
  
all 2351 items...

Prader-Willi habitus, osteopenia, and camptodactyly [MESH:C538276] (1)   
MESH:C538276
 Prader-Willi habitus, osteopenia, and camptodactyly
C538276
 
  
  
  

Premature aging, Okamoto type [MESH:C535270] (1)   
MESH:C535270
 Premature aging, Okamoto type
C535270
 
  
  
  

Singleton Merten syndrome [MESH:C537343] (1)   
MESH:C537343
 Singleton Merten syndrome
C537343
 
  
  
  

Winchester syndrome [MESH:C536709] (1)   
MESH:C536709
 Winchester syndrome
C536709
 
  
  
  

 (others) (669)   
MESH:C000666
 coralyne
C000666
 
  
  
  
MESH:C001570
 alexidine
C001570
 
  
  
  
MESH:C001765
 cyhexatin
C001765
 
  
  
  
MESH:C002010
 4-(2-aminoethyl)benzenesulfonylfluoride
C002010
 
  
  
  
MESH:C002029
 17alpha-ethynylestr-5(10)-ene-3alpha,17beta-diol
C002029
 
  
  
  
MESH:C002448
 1,2-linoleoylphosphatidylcholine
C002448
 
  
  
  
all 669 items...