Carney complex
(Q1044007)
autosomal dominant disease characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity
autosomal dominant disease characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity
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Current Data About
Carney complex
| (P31) |
(Q42303753)
(Q929833) (Q112193867) |
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| (P279) |
(Q18553439)
(Q18987129)
(Q5196705) (Q179630)
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| (P1325) |
http://www.nanbyou.or.jp/entry/4753
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| (P1748) |
C4705
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| (P1889) |
(Q5044023)
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| (P1995) |
(Q162555)
(Q10379) |
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| (P2293) |
(Q18030765)
(Q18029745)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0050471
http://identifiers.org/doid/DOID:0050471
http://www.orpha.net/ORDO/Orphanet_1359 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
Carney Complex, Type 1 Carney Complex, Type 2 Carney Syndrome LAMB Syndrome NAME Syndrome Carney complex variant CARNEY COMPLEX, TYPE 1; CNC1 Myxoma, Spotty Pigmentation, and Endocrine Overactivity Carney Myxoma-Endocrine Complex CNC1 |
| description | autosomal dominant disease characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity |
External Links