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's subclass of is recorded as hypothyroidism, congenital, nongoitrous[3].
- congenital nongoitrous hypothryoidism 6's subclass of is recorded as genetic disease[4].
- congenital nongoitrous hypothryoidism 6's subclass of is recorded as autosomal dominant disease[5].
- congenital nongoitrous hypothryoidism 6's OMIM ID is recorded as 614450[6].
- congenital nongoitrous hypothryoidism 6's Disease Ontology ID is recorded as DOID:0070128[7].
- congenital nongoitrous hypothryoidism 6's genetic association is recorded as THRA[8].
- congenital nongoitrous hypothryoidism 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070128[9].
- congenital nongoitrous hypothryoidism 6's exact match is recorded as http://identifiers.org/doid/DOID:0070128[10].
- congenital nongoitrous hypothryoidism 6's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_97927[11].
- congenital nongoitrous hypothryoidism 6's UMLS CUI is recorded as C3280817[12].
- congenital nongoitrous hypothryoidism 6's ICD-10-CM is recorded as E03.1[13].
- congenital nongoitrous hypothryoidism 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- congenital nongoitrous hypothryoidism 6's Mondo ID is recorded as MONDO_0013757[15].
- congenital nongoitrous hypothryoidism 6's UniProt disease ID is recorded as DI-03343[16].