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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Chromosome Disorders > Rubinstein-Taybi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Chromosome Disorders > Rubinstein-Taybi Syndrome
... > Pathological Conditions, Signs and Symptoms > Signs and Symptoms > Neurologic Manifestations > Neurobehavioral Manifestations > Intellectual Disability > Rubinstein-Taybi Syndrome
Nervous System Diseases > Neurologic Manifestations > Neurobehavioral Manifestations > Intellectual Disability > Rubinstein-Taybi Syndrome
Behavior and Behavior Mechanisms > Neurobehavioral Manifestations > Intellectual Disability > Rubinstein-Taybi Syndrome
Mental Disorders > Neurodevelopmental Disorders > Intellectual Disability > Rubinstein-Taybi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Rubinstein-Taybi Syndrome
Musculoskeletal Diseases > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Rubinstein-Taybi Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Rubinstein-Taybi Syndrome
Musculoskeletal Diseases > Bone Diseases > Bone Diseases, Developmental > Dysostoses > Rubinstein-Taybi Syndrome

Preferred term

Rubinstein-Taybi Syndrome  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Broad Thumb Hallux Syndrome
  • Broad Thumb-Hallux Syndrome
  • Broad Thumb-Hallux Syndromes
  • Broad Thumbs and Great Toes, Characteristic Facies, and Mental Retardation
  • Rubinstein Syndrome
  • Syndrome, Broad Thumb-Hallux
  • Syndrome, Rubinstein
  • Syndromes, Broad Thumb-Hallux

Scope note

  • A chromosomal disorder characterized by MENTAL RETARDATION, broad thumbs, webbing of fingers and toes, beaked nose, short upper lip, pouting lower lip, agenesis of corpus callosum, large foramen magnum, keloid formation, pulmonary stenosis, vertebral anomalies, chest wall anomalies, sleep apnea, and megacolon. The disease has an autosomal dominant pattern of inheritance and is associated with deletions of the short arm of chromosome 16 (16p13.3).

History note

  • 91(72); was see under ABNORMALITIES, MULTIPLE 1972-90

In other languages

URI

http://www.yso.fi/onto/mesh/D012415

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