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- B1135f8bedb108bae9efd56b6a6bdd35e hasDbXref "Orphanet:1296" @default.
- B1135f8bedb108bae9efd56b6a6bdd35e type Axiom @default.
- B1135f8bedb108bae9efd56b6a6bdd35e annotatedProperty IAO_0000115 @default.
- B1135f8bedb108bae9efd56b6a6bdd35e annotatedSource MONDO_0009507 @default.
- B1135f8bedb108bae9efd56b6a6bdd35e annotatedTarget "Lambert syndrome is a very rare syndrome described in four sibs of one French family and characterized by branchial dysplasia (malar hypoplasia, macrostomia, preauricular tags and meatal atresia), club feet, inguinal herniae and cholestasis due to paucity of interlobular bile ducts and intellectual deficit." @default.