# congenital nongoitrous hypothryoidism 6

> congenital hypothyroidism that has material basis in heterozygous mutation in the THRA gene on chromosome 17q21.1

**Wikidata**: [Q50349694](https://www.wikidata.org/wiki/Q50349694)  
**Source**: https://4ort.xyz/entity/congenital-nongoitrous-hypothryoidism-6


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)