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- NCIT_C129719 IAO_0000115 "A condition caused by the presence of an extra Y chromosome resulting in 47,XYY karyotype in an individual with male phenotype. The condition is characterized by tall stature, increased risk of learning disabilities, and delayed development of speech and language. Testicular function and size are normal." @default.
- NCIT_C129719 NCIT_NHC0 "C129719" @default.
- NCIT_C129719 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C129719 NCIT_P108 "47,XYY Syndrome" @default.
- NCIT_C129719 NCIT_P200 "C28193" @default.
- NCIT_C129719 NCIT_P310 "Retired_Concept" @default.
- NCIT_C129719 NCIT_P98 "Wed May 24 14:13:00 EDT 2017 - See 'XYY Syndrome(C85237)'" @default.
- NCIT_C129719 normalizedInformationContent "100" @default.
- NCIT_C129719 referenceCount "1" @default.
- NCIT_C129719 hasExactSynonym "47,XYY Syndrome" @default.
- NCIT_C129719 hasExactSynonym "47,XYY" @default.
- NCIT_C129719 hasExactSynonym "XYY Syndrome" @default.
- NCIT_C129719 type Class @default.
- NCIT_C129719 isDefinedBy ncit.owl @default.
- NCIT_C129719 label "47,XYY Syndrome" @default.
- NCIT_C129719 subClassOf NCIT_C129719 @default.
- NCIT_C129719 subClassOf NCIT_C143136 @default.
- NCIT_C129719 subClassOf NCIT_C28428 @default.
- NCIT_C129719 deprecated "true" @default.