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Items: 5

1.

Thyroid hormone resistance, generalized, autosomal dominant

Generalized thyroid hormone resistance is characterized by elevated serum levels of free thyroid hormones with inappropriately elevated thyroid-stimulating hormone (TSH) as well as clinical and biochemical evidence of decreased thyroid hormone action. Affected individuals also show unresponsiveness to large doses of exogenous thyroid hormones (summary by Parrilla et al., 1991). [from OMIM]

MedGen UID:
424846
Concept ID:
C2937288
Disease or Syndrome
2.

Thyroid hormone resistance, generalized, autosomal recessive

A rare, autosomal recessive inherited disorder usually caused by mutations in the THRB gene. It is characterized by a defective physiological resistance to thyroid hormones, resulting in the elevation of thyroxin and triiodothyronine in the serum. [from MONDO]

MedGen UID:
483749
Concept ID:
C3489796
Disease or Syndrome
3.

Selective pituitary resistance to thyroid hormone

Selective pituitary resistance to thyroid hormone (PRTH) results in continued thyroid-stimulating hormone (TSH) production driving hypersecretion of T3 and T4 to establish a new equilibrium, with high serum levels of free thyroid hormones together with a nonsuppressed TSH. The presence of a variety of thyrotoxic features, including palpitations, anxiety, tremor, heat intolerance, insomnia, weight loss, and increased stool frequency, suggests that peripheral tissues are less refractory to thyroid hormones than the pituitary (summary by Adams et al., 1994). [from OMIM]

MedGen UID:
333543
Concept ID:
C1840364
Disease or Syndrome
4.

Congenital nongoitrous hypothryoidism 6

Any hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the THRA gene. [from MONDO]

MedGen UID:
482447
Concept ID:
C3280817
Disease or Syndrome
5.

Generalized resistance to thyroid hormone

Reduced sensitivity of end organs to thyroid hormone characterized by elevated serum levels of free thyroid hormone with nonsuppressed thyroid stimulating hormone. [from HPO]

MedGen UID:
1654700
Concept ID:
C4722330
Disease or Syndrome
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