(Q50349694)
English
congenital nongoitrous hypothryoidism 6
A congenital hypothyroidism that has material basis in heterozygous mutation in the THRA gene on chromosome 17q21.1.
- CHNG6
- HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6
- HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6
- Hypothyroidism, Congenital, Nongoitrous, type 6
- congenital nongoitrous hypothyroidism 6
Statements
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Identifiers
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