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C05. Musculoskeletal Diseases: all > Musculoskeletal Diseases [MESH:D009140] > Bone Diseases [MESH:D001847] > Bone Diseases, Developmental [MESH:D001848] > Dysostoses [MESH:D004413] > Synostosis [MESH:D013580] > Craniosynostoses [MESH:D003398]

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

Acrocephalosyndactylia [MESH:D000168] (201)   
MESH:C004925
 methylmercuric chloride
C004925
 
  
  
  
MESH:C005277
 alpha-naphthyl thiourea
C005277
 
  
  
  
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006326
 fluprostenol
C006326
 
  
  
  
MESH:C006632
 arsenic trioxide
C006632
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
all 201 items...

Aurocephalosyndactyly [MESH:C566235] (1)   
MESH:C566235
 Aurocephalosyndactyly
C566235
 
  
  
  

Baraitser Rodeck Garner syndrome [MESH:C537906] (1)   
MESH:C537906
 Baraitser Rodeck Garner syndrome
C537906
 
  
  
  

Bohring syndrome [MESH:C537419] (26)   
MESH:C015559
 trimellitic anhydride
C015559
 
  
  
  
MESH:C044887
 beta-methylcholine
C044887
 
  
  
  
MESH:C045950
 propiconazole
C045950
 
  
  
  
MESH:C495626
 14-deoxy-11,12-didehydroandrographolide
C495626
 
  
  
  
MESH:C517041
 (4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II)
C517041
 
  
  
  
MESH:C537419
 Bohring syndrome
C537419
 
  
  
  
all 26 items...

Calabro syndrome [MESH:C537960] (1)   
MESH:C537960
 Calabro syndrome
C537960
 
  
  
  

Cole Carpenter syndrome [MESH:C535963] (1)   
MESH:C535963
 Cole Carpenter syndrome
C535963
 
  
  
  

Cranioectodermal Dysplasia [MESH:C562966] (16)   
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C009505
 4,4'-diaminodiphenylmethane
C009505
 
  
  
  
MESH:C012589
 trichostatin A
C012589
 
  
  
  
MESH:C029497
 2,3-bis(3'-hydroxybenzyl)butyrolactone
C029497
 
  
  
  
MESH:C045362
 prochloraz
C045362
 
  
  
  
all 16 items...

Craniometaphyseal dysplasia, autosomal recessive type [MESH:C536570] (1)   
MESH:C536570
 Craniometaphyseal dysplasia, autosomal recessive type
C536570
 
  
  
  

Craniosynostosis Mental Retardation Clefting Syndrome [MESH:C565663] (1)   
MESH:C565663
 Craniosynostosis Mental Retardation Clefting Syndrome
C565663
 
  
  
  

Craniosynostosis Microcephaly with Chromosomal Breakage and Other Abnormalities [MESH:C565667] (1)   
MESH:C565667
 Craniosynostosis Microcephaly with Chromosomal Breakage and Other Abnormalities
C565667
 
  
  
  

Craniosynostosis radial aplasia syndrome [MESH:C536788] (30)   
MESH:C015559
 trimellitic anhydride
C015559
 
  
  
  
MESH:C016403
 2,4-dinitrotoluene
C016403
 
  
  
  
MESH:C023514
 2,6-dinitrotoluene
C023514
 
  
  
  
MESH:C025462
 sulindac sulfide
C025462
 
  
  
  
MESH:C025589
 ochratoxin A
C025589
 
  
  
  
MESH:C029497
 2,3-bis(3'-hydroxybenzyl)butyrolactone
C029497
 
  
  
  
all 30 items...

Craniosynostosis Syndrome, Autosomal Recessive [MESH:C564700] (1)   
MESH:C564700
 Craniosynostosis Syndrome, Autosomal Recessive
C564700
 
  
  
  

Craniosynostosis with Anomalies of the Cranial Base and Digits [MESH:C565666] (1)   
MESH:C565666
 Craniosynostosis with Anomalies of the Cranial Base and Digits
C565666
 
  
  
  

Craniosynostosis with Ectopia Lentis [MESH:C566357] (1)   
MESH:C566357
 Craniosynostosis with Ectopia Lentis
C566357
 
  
  
  

Craniosynostosis with Fibular Aplasia [MESH:C565665] (1)   
MESH:C565665
 Craniosynostosis with Fibular Aplasia
C565665
 
  
  
  

Craniosynostosis with Ocular Abnormalities and Hallucal Defects [MESH:C564263] (1)   
MESH:C564263
 Craniosynostosis with Ocular Abnormalities and Hallucal Defects
C564263
 
  
  
  

Craniosynostosis, Adelaide Type [MESH:C563471] (1)   
MESH:C563471
 Craniosynostosis, Adelaide Type
C563471
 
  
  
  

Craniosynostosis, anal anomalies, and porokeratosis [MESH:C536789] (1)   
MESH:C536789
 Craniosynostosis, anal anomalies, and porokeratosis
C536789
 
  
  
  

Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism [MESH:C564241] (1)   
MESH:C564241
 Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism
C564241
 
  
  
  

Craniosynostosis, Philadelphia Type [MESH:C563368] (1)   
MESH:C563368
 Craniosynostosis, Philadelphia Type
C563368
 
  
  
  

Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus [MESH:C536790] (1)   
MESH:C536790
 Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus
C536790
 
  
  
  

Craniosynostosis, Type 2 [MESH:C565753] (36)   
MESH:C006632
 arsenic trioxide
C006632
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C007076
 citral
C007076
 
  
  
  
MESH:C008261
 lead acetate
C008261
 
  
  
  
MESH:C009166
 retinol acetate
C009166
 
  
  
  
MESH:C018021
 cobaltous chloride
C018021
 
  
  
  
all 36 items...

Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig [MESH:C565664] (1)   
MESH:C565664
 Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig
C565664
 
  
  
  

Craniotelencephalic dysplasia [MESH:C535597] (1)   
MESH:C535597
 Craniotelencephalic dysplasia
C535597
 
  
  
  

Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)   
MESH:C005277
 alpha-naphthyl thiourea
C005277
 
  
  
  
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006326
 fluprostenol
C006326
 
  
  
  
MESH:C006632
 arsenic trioxide
C006632
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C007164
 cumene hydroperoxide
C007164
 
  
  
  
all 85 items...

Fine-Lubinsky syndrome [MESH:C537933] (1)   
MESH:C537933
 Fine-Lubinsky syndrome
C537933
 
  
  
  

Furlong syndrome [MESH:C538192] (1)   
MESH:C538192
 Furlong syndrome
C538192
 
  
  
  

Genoa syndrome [MESH:C537684] (1)   
MESH:C537684
 Genoa syndrome
C537684
 
  
  
  

Hordnes Engebretsen Knudtson syndrome [MESH:C536067] (1)   
MESH:C536067
 Hordnes Engebretsen Knudtson syndrome
C536067
 
  
  
  

Hunter-McAlpine syndrome [MESH:C536072] (1)   
MESH:C536072
 Hunter-McAlpine syndrome
C536072
 
  
  
  

Iida Kannari syndrome [MESH:C536284] (1)   
MESH:C536284
 Iida Kannari syndrome
C536284
 
  
  
  

Jackson-Weiss syndrome [MESH:C537559] (149)   
MESH:C004925
 methylmercuric chloride
C004925
 
  
  
  
MESH:C005277
 alpha-naphthyl thiourea
C005277
 
  
  
  
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006326
 fluprostenol
C006326
 
  
  
  
MESH:C006632
 arsenic trioxide
C006632
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
all 149 items...

Kleeblattschaedel syndrome [MESH:C536884] (2)   
MESH:C536884
 Kleeblattschaedel syndrome
C536884
 
  
  
  
MESH:D003042
 Cocaine
D003042
 
  
  
  

Lowry Maclean syndrome [MESH:C537037] (1)   
MESH:C537037
 Lowry Maclean syndrome
C537037
 
  
  
  

Mehta Lewis Patton syndrome [MESH:C536147] (1)   
MESH:C536147
 Mehta Lewis Patton syndrome
C536147
 
  
  
  

Muenke Syndrome [MESH:C537369] (66)   
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C007350
 nitrofen
C007350
 
  
  
  
MESH:C009166
 retinol acetate
C009166
 
  
  
  
MESH:C010176
 halofuginone
C010176
 
  
  
  
MESH:C011890
 kojic acid
C011890
 
  
  
  
all 66 items...

Oculopalatoskeletal syndrome [MESH:C537738] (45)   
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C008261
 lead acetate
C008261
 
  
  
  
MESH:C009505
 4,4'-diaminodiphenylmethane
C009505
 
  
  
  
MESH:C012568
 terbufos
C012568
 
  
  
  
MESH:C014347
 decitabine
C014347
 
  
  
  
MESH:C015559
 trimellitic anhydride
C015559
 
  
  
  
all 45 items...

Opitz trigonocephaly syndrome [MESH:C537418] (1)   
MESH:C537418
 Opitz trigonocephaly syndrome
C537418
 
  
  
  

Pfeiffer Tietze Welte syndrome [MESH:C537891] (1)   
MESH:C537891
 Pfeiffer Tietze Welte syndrome
C537891
 
  
  
  

Piepkorn Karp Hickok syndrome [MESH:C535774] (1)   
MESH:C535774
 Piepkorn Karp Hickok syndrome
C535774
 
  
  
  

Plagiocephaly and X-linked mental retardation [MESH:C537512] (1)   
MESH:C537512
 Plagiocephaly and X-linked mental retardation
C537512
 
  
  
  

Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism , and Brachymelia [MESH:C564881] (1)   
MESH:C564881
 Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism , and Brachymelia
C564881
 
  
  
  

Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)   
MESH:C005277
 alpha-naphthyl thiourea
C005277
 
  
  
  
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006326
 fluprostenol
C006326
 
  
  
  
MESH:C006632
 arsenic trioxide
C006632
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C007164
 cumene hydroperoxide
C007164
 
  
  
  
all 85 items...

Shprintzen Golberg craniosynostosis [MESH:C537328] (76)   
MESH:C005961
 bis(tri-n-butyltin)oxide
C005961
 
  
  
  
MESH:C008261
 lead acetate
C008261
 
  
  
  
MESH:C010176
 halofuginone
C010176
 
  
  
  
MESH:C014476
 diethyl maleate
C014476
 
  
  
  
MESH:C015559
 trimellitic anhydride
C015559
 
  
  
  
MESH:C017947
 sodium arsenite
C017947
 
  
  
  
all 76 items...

Skeletal dysplasia, San Diego type [MESH:C536670] (1)   
MESH:C536670
 Skeletal dysplasia, San Diego type
C536670
 
  
  
  

Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation [MESH:C566515] (1)   
MESH:C566515
 Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation
C566515
 
  
  
  

Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet [MESH:C564759] (1)   
MESH:C564759
 Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet
C564759
 
  
  
  

Trigonocephaly, Nonsyndromic [MESH:C562951] (1)   
MESH:C562951
 Trigonocephaly, Nonsyndromic
C562951
 
  
  
  

Warman Mulliken Hayward syndrome [MESH:C536684] (1)   
MESH:C536684
 Warman Mulliken Hayward syndrome
C536684
 
  
  
  

 (others) (85)   
MESH:C002010
 4-(2-aminoethyl)benzenesulfonylfluoride
C002010
 
  
  
  
MESH:C002963
 geranylgeranyl pyrophosphate
C002963
 
  
  
  
MESH:C004808
 farnesyl pyrophosphate
C004808
 
  
  
  
MESH:C007095
 cobaltiprotoporphyrin
C007095
 
  
  
  
MESH:C011272
 perfosfamide
C011272
 
  
  
  
MESH:C012258
 mevastatin
C012258
 
  
  
  
all 85 items...