Name | Distal arthrogryposis type 2B |
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Synonyms | Arthrogryposis, distal, type 2b | Arthrogryposis multiplex congenita, distal, type 2b | Arthrogryposis Multiplex Congenita, Distal, Type II, with Craniofacial Abnormalities | Arthrogryposis multiplex congenita type 2B | DA2B | Freeman-Sheldon Syndrome Variant | FSSV | Sheldon-Hall syndrome | SHS |
Categories | Congenital abnormality | Musculoskeletal disease |
MeSH® ID | C538400 |
OMIM® ID | 601680 |
1. |
Diseases
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Musculoskeletal Diseases
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2. |
Diseases
←
Musculoskeletal Diseases
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3. |
Diseases
←
Musculoskeletal Diseases
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4. |
Diseases
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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