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- Bcb54d212d9a111d4d2c670a1abfe766b hasDbXref "Orphanet:306498" @default.
- Bcb54d212d9a111d4d2c670a1abfe766b type Axiom @default.
- Bcb54d212d9a111d4d2c670a1abfe766b annotatedProperty IAO_0000115 @default.
- Bcb54d212d9a111d4d2c670a1abfe766b annotatedSource MONDO_0017623 @default.
- Bcb54d212d9a111d4d2c670a1abfe766b annotatedTarget "A group of clinically heterogeneous disorders united by a germline PTEN mutation and the involvement of derivatives of all 3 germ cell layers, manifesting with hamartomas, overgrowth and neoplasia. Currently, subsets carrying clinical diagnoses of Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, Proteus and Proteus-like syndromes and SOLAMEN syndrome belong to PHTS." @default.