Pfeiffer syndrome (Q1286848)
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acrocephalosyndactylia that has material basis in mutations in the FGFR1 and FGFR2 gene which results in premature fusion located in skull
- acrocephalosyndactylia type V
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Pfeiffer syndrome |
acrocephalosyndactylia that has material basis in mutations in the FGFR1 and FGFR2 gene which results in premature fusion located in skull |
|
Statements
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17 May 2019
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Pfeiffer syndrome
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Identifiers
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Sitelinks
Wikipedia(18 entries)
- arwiki متلازمة فايفر
- bswiki Pfeifferov sindrom
- dewiki Pfeiffer-Syndrom
- elwiki Σύνδρομο Pfeiffer
- enwiki Pfeiffer syndrome
- eswiki Síndrome de Pfeiffer
- fiwiki Pfeifferin oireyhtymä
- frwiki Syndrome de Pfeiffer
- idwiki Sindrom Pfeiffer
- itwiki Sindrome di Pfeiffer
- kkwiki Пфайффер синдромы
- nlwiki Syndroom van Pfeiffer
- plwiki Zespół Pfeiffera
- ptwiki Síndrome de Pfeiffer
- ruwiki Синдром Пфайффера
- svwiki Pfeiffers syndrom
- trwiki Pfeiffer sendromu
- ukwiki Синдром Пфайффера
Wikibooks(0 entries)
Wikinews(0 entries)
Wikiquote(0 entries)
Wikisource(0 entries)
Wikiversity(0 entries)
Wikivoyage(0 entries)
Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Pfeiffer syndrome