Antley-Bixler syndrome (Q585011)
autosomal recessive disease that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene
- trapezoidocephaly-synostosis syndrome
| Language | Label | Description | Also known as |
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| English |
Antley-Bixler syndrome
|
autosomal recessive disease that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene
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Statements
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Identifiers
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Sitelinks
Wikipedia(7 entries)
- dewiki Antley-Bixler-Syndrom
- enwiki Antley–Bixler syndrome
- fawiki سندرم آنتلی-بیکسلر
- fiwiki Antley–Bixlerin oireyhtymä
- plwiki Zespół Antleya-Bixlera
- ukwiki Синдром Антлі—Бікслера
- zhwiki 安特利－比克斯勒症候群
