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Related terms:
congenital abnormality
chromosome disorder
goiter
hyperthyroidism
hyperthyroxinemia
hypothyroidism
Situs Inversus
thyroid disease
thyroid neoplasm
Congenital Abnormality
thyroid dysgenesis
Subclass of:
Congenital Abnormality; Thyroid Diseases
Definitions related to thyroid dysgenesis:
  • A congenital condition characterized by hypoplasia, absence, or ectopic position of the thyroid gland. It is manifested with congenital hypoparathyroidism.
    NCI
    U.S. National Cancer Institute, 2021
  • Defective development of the THYROID GLAND. This concept includes thyroid agenesis (aplasia), hypoplasia, or an ectopic gland. Clinical signs usually are those of CONGENITAL HYPOTHYROIDISM.
    NLM Medical Subject Headings
    U.S. National Library of Medicine, 2025
  • Thyroid hypoplasia is a form of thyroid dysgenesis (see this term) characterized by incomplete development of the thyroid gland that results in primary congenital hypothyroidism (see this term), a permanent thyroid deficiency that is present from birth.
    NIH Genetic and Rare Diseases
    National Center for Advancing Translational Sciences
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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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