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Results 1 - 10 of 77 for hypothyroidism OR alopecia
  1. Alopecia areata 
    Alopecia areata is a common disorder that causes hair loss. "Alopecia" is a Latin term that means baldness, and "areata" refers to the patchy nature of the hair ...
    https://medlineplus.gov/genetics/condition/alopecia-areata - Genetics
  2. Androgenetic alopecia 
    Androgenetic alopecia is a common form of hair loss in both men and women. In men, it is also known as male pattern baldness, and in women, it is also known as female ...
    https://medlineplus.gov/genetics/condition/androgenetic-alopecia - Genetics
  3. Congenital hypothyroidism 
    Congenital hypothyroidism is a partial or complete loss of function of the thyroid gland (hypothyroidism) that affects infants from birth (congenital). The thyroid ...
    https://medlineplus.gov/genetics/condition/congenital-hypothyroidism - Genetics
  4. T-cell immunodeficiency, congenital alopecia, and nail dystrophy 
    T-cell immunodeficiency, congenital alopecia, and nail dystrophy is a type of severe combined immunodeficiency (SCID), which is a group of disorders characterized ...
    https://medlineplus.gov/...cy-congenital-alopecia-and-nail-dystrophy - Genetics
  5. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy 
    ... characteristic features of CARASIL include premature hair loss (alopecia) and attacks of low back pain. The hair ... CARASIL Familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertension Maeda syndrome Nemoto ...
    https://medlineplus.gov/...cortical-infarcts-and-leukoencephalopathy - Genetics
  6. Allan-Herndon-Dudley syndrome 
    Allan-Herndon-Dudley syndrome is a rare disorder of brain development that causes moderate to severe intellectual disability and problems with movement. This ...
    https://medlineplus.gov/.../condition/allan-herndon-dudley-syndrome - Genetics
  7. TSHB gene 
    ... least 10 TSHB gene mutations involved in congenital hypothyroidism, a condition characterized by abnormally low levels of ... a form of the condition called central congenital hypothyroidism, which occurs when stimulation of thyroid hormone production ...
    https://medlineplus.gov/genetics/gene/tshb - Genetics
  8. Brain-lung-thyroid syndrome 
    ... individuals have reduced thyroid function from birth (congenital hypothyroidism), resulting in lower-than-normal levels of thyroid ... have a milder condition called compensated or subclinical hypothyroidism, in which thyroid hormone levels are within the ...
    https://medlineplus.gov/.../condition/brain-lung-thyroid-syndrome - Genetics
  9. TSHR gene 
    ... mutations have been identified in people with congenital hypothyroidism, a condition characterized by abnormally low levels of ... levels remain low, causing mild to severe congenital hypothyroidism. Impaired thyroid stimulating hormone receptors may also disrupt ...
    https://medlineplus.gov/genetics/gene/tshr - Genetics
  10. TG gene 
    ... Mutations in the TG gene can cause congenital hypothyroidism, a condition characterized by abnormally low levels of ... not have other signs and symptoms of congenital hypothyroidism (described above). It is unclear why enlargement of ...
    https://medlineplus.gov/genetics/gene/tg - Genetics
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