- Autosomal dominant hereditary disorder (disorder)
- Camptodactyly (disorder)
- Congenital abnormal shape of digit (disorder)
- Congenital anomaly of musculoskeletal system (disorder)
- Congenital deformity
- Finding of musculoskeletal structure of finger (finding)
- Hereditary disorder of musculoskeletal system
- Inherited aminoaciduria
- Multiple malformation syndrome with limb defect as major feature
Name: Camptodactyly taurinuria syndrome (disorder)
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- Camptodactyly taurinuria syndrome (disorder)
- Camptodactyly taurinuria syndrome
- Familial streblodactyly with amino-aciduria
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Concept ID: 733466005- Camptodactyly taurinuria syndrome
- Familial streblodactyly with amino-aciduria
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ICD-10 Codes: Q681