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- Be38976dad19c16d6d4041843da10e6ae hasDbXref "Orphanet:1116" @default.
- Be38976dad19c16d6d4041843da10e6ae type Axiom @default.
- Be38976dad19c16d6d4041843da10e6ae annotatedProperty IAO_0000115 @default.
- Be38976dad19c16d6d4041843da10e6ae annotatedSource MONDO_0008808 @default.
- Be38976dad19c16d6d4041843da10e6ae annotatedTarget "Aplasia cutis congenita - intestinal lymphangiectasia is an extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterized by aplasia cutis congenita of the vertex and generalized edema (as well as hypoproteinemia and lymphopenia) due to intestinal lymphangiectasia. There have been no further descriptions in the literature since 1985." @default.