Allan-Herndon-Dudley syndrome (Q4731121)
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congenital disorder of nervous system
- ALLAN-HERNDON SYNDROME
- ALLAN-HERNDON-DUDLEY SYNDROME
- T3 Resistance
- X-linked intellectual disability-hypotonia syndrome
- Monocarboxylate transporter 8 deficiency
- AHDS
- MCT8 deficiency
- ALLAN-HERNDON-DUDLEY SYNDROME; AHDS
- MCT8-Specific Thyroid Hormone Cell Membrane Transporter Deficiency
- Mental Retardation, X-Linked, With Hypotonia
- Monocarboxylate transporter-8 deficiency
- Triiodothyronine resistence
- X-linked intellectual disability with hypotonia
- Triiodothyronine Resistance
- Mental Retardation and Muscular Atrophy
- T3 resisitence
- Intellectual disability and muscular atrophy
Language | Label | Description | Also known as |
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English | Allan-Herndon-Dudley syndrome |
congenital disorder of nervous system |
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C118843
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Identifiers
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Sitelinks
Wikipedia(6 entries)
- arwiki متلازمة آلان هيرندون دودلي
- dewiki Allan-Herndon-Dudley-Syndrom
- enwiki Allan–Herndon–Dudley syndrome
- fiwiki Allan–Herndonin oireyhtymä
- itwiki Sindrome di Allan-Herndon-Dudley
- ukwiki Синдром Аллана — Герндона — Дадлі