Thyroid dyshormonogenesis (Q7799748)
Jump to navigation
Jump to search
Familial thyroid dyshormonogenesis is a type of primary congenital hypothyroidism (see this term), a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis
- dyshormogenetic goiter
- TDH1
- Dyshormonogenesis
- THYROID DYSHORMONOGENESIS 1
- Hypothyroidism, Congenital, Due to Dyshormonogenesis, 1
- Thyroid Dyshormonogenesis type 1
- THYROID DYSHORMONOGENESIS 1; TDH1
- Iodine Accumulation, Transport, or Trapping Defect
- Thyroid Hormonogenesis, Genetic Defect In, 1
Language | Label | Description | Also known as |
---|---|---|---|
English | Thyroid dyshormonogenesis |
Familial thyroid dyshormonogenesis is a type of primary congenital hypothyroidism (see this term), a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis |
|
Statements
1 reference
2 references
C121751
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(3 entries)
- arwiki خلل تكون هرمونات الدرقية
- enwiki Thyroid dyshormonogenesis
- itwiki Dismorfogenesi tiroidea