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Musculoskeletal Diseases > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Cleidocranial Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Cleidocranial Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Osteochondrodysplasias > Cleidocranial Dysplasia
Musculoskeletal Diseases > Bone Diseases > Bone Diseases, Developmental > Osteochondrodysplasias > Cleidocranial Dysplasia

Término preferido

Cleidocranial Dysplasia  

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Tipo

  • mesh:Descriptor

Definición

  • Autosomal dominant syndrome in which there is delayed closing of the CRANIAL FONTANELLES; complete or partial absence of the collarbones (CLAVICLES); wide PUBIC SYMPHYSIS; short middle phalanges of the fifth fingers; and dental and vertebral anomalies.

Concepto genérico

Etiquetas alternativas

  • Cleidocranial Digital Dysostosis
  • Cleidocranial Dysostosis
  • Dysostosis, Cleidocranial
  • Marie-Sainton Syndrome
  • Scheuthauer-Marie-Sainton Syndrome

En otras lenguas

  • Dysostose cleido-crânienne héréditaire

    francés

  • Dysplasie cléido-crânienne
  • Hydrocéphalie héréditaire
  • Syndrome de Pierre Marie et Sainton
  • Syndrome de Scheuthauer
  • Syndrome de Scheuthauer-Marie-Sainton

URI

http://data.loterre.fr/ark:/67375/JVR-CCB3QFVH-T

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