PedAM
Pediatric Disease Annotations & Medicines
| Disease | cystic fibrosis |
| Phenotype | C0342199|iodine deficiency |
| Sentences | 1 |
| PubMedID- 26261983 | Variants in the cftr gene are known to cause cystic fibrosis, often comorbid with iodine deficiency and subclinical hypothyroidism [65, 66], thereby indicating a potential functional link to our phenotype of interest. |
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