Meckel syndrome (Q1915681)
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a rare, lethal, ciliopathic, genetic disorder with malformations of the urinary system, of central nervous system, hepatic developmental defects, and pulmonary hypoplasia.
- Meckel-Gruber syndrome
- Meckel–Gruber Syndrome
- Gruber Syndrome
- Dysencephalia Splanchnocystica
- Meckel's syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | No label defined |
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| English | Meckel syndrome |
a rare, lethal, ciliopathic, genetic disorder with malformations of the urinary system, of central nervous system, hepatic developmental defects, and pulmonary hypoplasia. |
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Statements
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753.1
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753.10
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C98978
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1 reference
Meckel syndrome
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Identifiers
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7 February 2022
Sitelinks
Wikipedia(12 entries)
- arwiki متلازمة ميكل-جروبر
- bswiki Meckelov sindrom
- dewiki Meckel-Syndrom
- enwiki Meckel–Gruber syndrome
- eswiki Síndrome de Meckel
- fiwiki Meckelin oireyhtymä
- frwiki Syndrome de Meckel
- itwiki Sindrome di Meckel
- plwiki Zespół Meckela
- ptwiki Síndrome de Meckel-Gruber
- ruwiki Синдром Меккеля — Грубера
- trwiki Meckel-Gruber sendromu
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:Meckel syndrome