Disease | hypothyroidism |
Phenotype | C0010308|congenital goitre |
Sentences | 2 |
PubMedID- 20447071 | congenital goitre with hypothyroidism caused by a novel compound heterozygous mutations in the thyroglobulin gene. |
PubMedID- 19438905 | Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. |
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