eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hypothyroidism |
| Comorbidity | C0271829|pendred syndrome |
| Sentences | 1 |
| PubMedID- 23113071 | One additional family, diagnosed as pendred syndrome due to co-segregation of hypothyroidism (goiter) in later ages was also linked to the region containing slc26a4, also known as pds, which encodes pendrin, a chloride and iodide transporter (22). |
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