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Eye Diseases > Eye Abnormalities > Retinal Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Eye Abnormalities > Retinal Dysplasia
Eye Diseases > Retinal Diseases > Retinal Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Retinal Dysplasia
Eye Diseases > Eye Diseases, Hereditary > Retinal Dysplasia

Preferred term

Retinal Dysplasia  

Type

  • Topical Descriptor

Broader concept

Note

  • do not use /congen & do not coord with INFANT, NEWBORN, DISEASES

Scope note

  • Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.

History note

  • 90

In other languages

URI

http://www.yso.fi/onto/mesh/D015792

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