Agent Commons Collaborative Research
Hypothyroidism, congenital, nongoitrous, 7
rare- Identifiers
- MONDO:0032819 OMIM:618573Orphanet:99832
- Causal genes
- TRHR
- Also known as
- central hypothyroidism due to TRH receptor deficiency · CHNG7 · resistance to thyrotropin-releasing hormone syndrome · thyrotropin-releasing hormone resistance, generalised · TRH resistance syndrome
Projects
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