congenital nongoitrous hypothryoidism 6
congenital hypothyroidism that has material basis in heterozygous mutation in the THRA gene on chromosome 17q21.1
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congenital nongoitrous hypothryoidism 6
Summary
congenital nongoitrous hypothryoidism 6 is a class of disease[1].
Key Facts
- congenital nongoitrous hypothryoidism 6's instance of is recorded as class of disease[2].
- congenital nongoitrous hypothryoidism 6 is a type of hypothyroidism, congenital, nongoitrous[3].
- congenital nongoitrous hypothryoidism 6 is a type of genetic disease[4].
- congenital nongoitrous hypothryoidism 6 is a type of autosomal dominant disease[5].
- congenital nongoitrous hypothryoidism 6's genetic association is recorded as THRA[6].
- congenital nongoitrous hypothryoidism 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070128[7].
- congenital nongoitrous hypothryoidism 6's exact match is recorded as http://identifiers.org/doid/DOID:0070128[8].
- congenital nongoitrous hypothryoidism 6's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_97927[9].
- congenital nongoitrous hypothryoidism 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].