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CD in Genetics Meaning

The CD meaning in Genetics terms is "Cluster Determinant". There are 4 related meanings of the CD Genetics abbreviation.

CD on Genetics Full Forms

  1. Cluster Determinant
  2. Campomelic Dysplasia A severe birth defect that affects the formation of the bones, genital organs, and facial features. Physical features of the condition typically include bowing of the long bones of the legs and sometimes the arms, characteristic dimpling of the skin over the abnormal bones, shortened legs, underdeveloped shoulder blades, dislocated hips, abnormally rotated feet (clubfeet), and an abnormal number of ribs.
  3. Celiac Disease A malabsorption syndrome that is precipitated by the ingestion of foods containing gluten, such as wheat, rye, and barley. It is characterized by inflammation of the small intestine, loss of microvilli structure, failed intestinal absorption, and malnutrition.
  4. Cone Degeneration

Frequently Asked Questions (FAQ)

  1. What does CD stand for Genetics?

    CD stands for Cone Degeneration in Genetics terms.

  2. What is the shortened form of Campomelic Dysplasia in Genetics?

    The short form of "Campomelic Dysplasia" is CD for Genetics.

Citation

CD in Genetics. Acronym24.com. (2022, March 30). Retrieved April 23, 2024 from https://acronym24.com/cd-meaning-in-genetics/

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