Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
congenital nongoitrous hypothryoidism 6
OMIM:614450
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
04/19/2021
PubMed IDs:
11734632 22168587 22494134 23633213 23940126 24969835 25670821 26037512 26782358 27144938 28471274 30753492 30842990 31589614 32204686 32349464 33509032
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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