LEOPARD syndrome (Q1798016)
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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
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | LEOPARD syndrome |
rare autosomal dominant,[3] multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene (PTPN11) |
|
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LEOPARD syndrome
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Identifiers
LEOPARD Syndrome
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Wikipedia(13 entries)
- arwiki متلازمة نونان ذات التصبغات المتعددة
- cawiki Síndrome LEOPARD
- dewiki LEOPARD-Syndrom
- enwiki Noonan syndrome with multiple lentigines
- eswiki Síndrome de Noonan con múltiples lentigos
- 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
- ruwiki Синдром LEOPARD
- trwiki LEOPARD sendromu
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Multilingual sites(1 entry)
- commonswiki Category:LEOPARD syndrome