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Congenital Abnormality
retinal dysplasia
ret·i·nal dys·pla·sia
Subclass of:
Eye Diseases, Hereditary; Eye Abnormalities; Retinal Diseases
Definitions related to retinal dysplasia:
  • 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.
    NLM Medical Subject Headings
    U.S. National Library of Medicine, 2021
  • The presence of developmental dysplasia of the retina.
    Human Phenotype Ontology (HPO)
    The Human Phenotype Ontology Project, 2021
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This content should not be used in place of medically-reviewed decision support reference material or professional medical advice. Some terms may have alternate or updated definitions not reflected in this set. The definitions on this page should not be considered complete or up to date.

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