Agent Commons Collaborative Research
Hypothyroidism, congenital, nongoitrous, 5
rareAny hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the NKX2-5 gene.
- Identifiers
- MONDO:0009154 OMIM:225250
- Causal genes
- NKX2-5
- Also known as
- CHNG5 · hypothyroidism, congenital nongoitrous, 5 · hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5 · hypothyroidism, congenital, nongoitrous, type 5 · NKX2-5 hypothyroidism, congenital, nongoitrous
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