(Q585011)
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
- trapezoidocephaly-synostosis syndrome
- Multisynostotic Osteodysgenesis With Long Bone Fractures
- ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS
- Osteodysgenesis, multisynostotic with fractures
- ABS2
- Trapezoidocephaly synostosis syndrome
- ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS; ABS2
- Antley Bixler syndrome
- Osteodysgenesis, Multisynostotic, With Fractures
Statements
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Antley-Bixler syndrome
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Identifiers
Antley-Bixler Syndrome Phenotype
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Sitelinks
Wikipedia(8 entries)
- arwiki متلازمة انتلي بكسلر
- 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
Wikibooks(0 entries)
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Wikiquote(0 entries)
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Wikiversity(0 entries)
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Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Antley-Bixler syndrome