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Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Hypothyroidism, congenital, nongoitrous
Hypothyroidism, congenital, nongoitrous, 8
rare
Identifiers
MONDO:0026731
OMIM:301033
Causal genes
TBL1X
Part of
Hypothyroidism, congenital, nongoitrous
Also known as
CHNG8
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