(Q1798016)
English
LEOPARD syndrome
rare autosomal dominant,[3] multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene (PTPN11)
- LEOPARD Syndrome
- Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome
- Cardiocutaneous syndrome
- Generalized lentiginosis (disorder)
- Gorlin syndrome II
- Lentiginosis profusa syndrome
- Moynahan syndrome
- Multiple lentigines syndrome (disorder)
- Progressive cardiomyopathic lentiginosis
- Multiple lentigines syndrome
- Generalized lentiginosis
- Noonan syndrome with multiple lentigines
Statements
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LEOPARD syndrome
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Identifiers
LEOPARD Syndrome
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Sitelinks
Wikipedia(12 entries)
- arwiki متلازمة نونان ذات التصبغات المتعددة
- cawiki Síndrome LEOPARD
- dewiki LEOPARD-Syndrom
- enwiki Noonan syndrome with multiple lentigines
- eswiki Síndrome LEOPARD
- frwiki Syndrome LEOPARD
- idwiki Sindrom Noonan dengan banyak lentigin
- itwiki Sindrome LEOPARD
- jawiki 多発性黒子を伴うヌーナン症候群
- kowiki 다발성 흑자 증후군
- plwiki Zespół LEOPARD
- trwiki LEOPARD sendromu
Wikibooks(0 entries)
Wikinews(0 entries)
Wikiquote(0 entries)
Wikisource(0 entries)
Wikiversity(0 entries)
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Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:LEOPARD syndrome