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PedAM

Pediatric Disease Annotations & Medicines




Disease hypothyroidism
Phenotype C0271829|pendred syndrome
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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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