Pendred syndrome (Q1707822)
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genetic disorder
- Pendred Syndrome
- TDH2B
- congenital hypothyroidism due to dyshormonogenesis 2B
- deafness with goiter
- genetic defect in thyroid hormonogenesis 2B
- goiter-deafness syndrome
- thyroid dyshormonogenesis 2B
- Hypothyroidism, Congenital, Due to Dyshormonogenesis, 2B
- Thyroid Hormonogenesis, Genetic Defect In, 2B
- PENDRED SYNDROME; PDS
- PDS
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Pendred syndrome |
genetic disorder |
|
Statements
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C121745
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Identifiers
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Sitelinks
Wikipedia(13 entries)
- arwiki متلازمة بيندريد
- bswiki Pendredov sindrom
- cswiki Pendredův syndrom
- dewiki Pendred-Syndrom
- enwiki Pendred syndrome
- eswiki Síndrome de Pendred
- fiwiki Pendredin oireyhtymä
- frwiki Syndrome de Pendred
- itwiki Sindrome di Pendred
- mkwiki Пендред синдром
- nlwiki Syndroom van Pendred
- plwiki Zespół Pendreda
- ruwiki Синдром Пендреда