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- NCIT_C3472 IAO_0000115 "X-linked or autosomal recessive disorder characterized by defects of both humoral and cell mediated immunity, resulting in low or absent antibody levels, leukopenia, marked susceptibility to infections, and early death.--2004" @default.
- NCIT_C3472 NCIT_NHC0 "C3472" @default.
- NCIT_C3472 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C3472 NCIT_P107 "Severe Combined Immunodeficiency" @default.
- NCIT_C3472 NCIT_P108 "Severe Combined Immunodeficiency" @default.
- NCIT_C3472 NCIT_P207 "C3806381" @default.
- NCIT_C3472 NCIT_P322 "CTRP" @default.
- NCIT_C3472 NCIT_P322 "Cellosaurus" @default.
- NCIT_C3472 NCIT_P322 "MedDRA" @default.
- NCIT_C3472 NCIT_P322 "NICHD" @default.
- NCIT_C3472 NCIT_P325 "A rare, inherited disease that is marked by a lack of B lymphocytes (white blood cells that make antibodies and help fight infections) and a lack of T lymphocytes (white blood cells that attack virus-infected cells, foreign cells, and cancer cells). Patients with this disease have a high risk of developing viral, bacterial, and fungal infections." @default.
- NCIT_C3472 NCIT_P325 "X-linked or autosomal recessive disorder characterized by defects of both humoral and cell mediated immunity, resulting in low or absent antibody levels, leukopenia, marked susceptibility to infections, and early death.--2004" @default.
- NCIT_C3472 NCIT_P366 "Severe_Combined_Immunodeficiency" @default.
- NCIT_C3472 NCIT_P375 "Severe combined immunodeficiency syndrome" @default.
- NCIT_C3472 NCIT_R116 NCIT_C150672 @default.
- NCIT_C3472 NCIT_R116 NCIT_C150673 @default.
- NCIT_C3472 NCIT_R116 NCIT_C26323 @default.
- NCIT_C3472 NCIT_R116 NCIT_C27351 @default.
- NCIT_C3472 NCIT_R116 NCIT_C27551 @default.
- NCIT_C3472 NCIT_R116 NCIT_C2991 @default.
- NCIT_C3472 NCIT_R116 NCIT_C35686 @default.
- NCIT_C3472 NCIT_R116 NCIT_C35814 @default.
- NCIT_C3472 NCIT_R116 NCIT_C7057 @default.
- NCIT_C3472 NCIT_R116 NCIT_C9308 @default.
- NCIT_C3472 normalizedInformationContent "74.383635266183077" @default.
- NCIT_C3472 referenceCount "48" @default.
- NCIT_C3472 hasExactSynonym "SCID" @default.
- NCIT_C3472 hasExactSynonym "Severe Combined Immune Deficiency" @default.
- NCIT_C3472 hasExactSynonym "Severe Combined Immunodeficiency" @default.
- NCIT_C3472 hasExactSynonym "severe combined immunodeficiency disease" @default.
- NCIT_C3472 inSubset NCIT_C116977 @default.
- NCIT_C3472 inSubset NCIT_C118168 @default.
- NCIT_C3472 inSubset NCIT_C118464 @default.
- NCIT_C3472 inSubset NCIT_C165258 @default.
- NCIT_C3472 inSubset NCIT_C189762 @default.
- NCIT_C3472 inSubset NCIT_C192842 @default.
- NCIT_C3472 inSubset NCIT_C90259 @default.
- NCIT_C3472 type Class @default.
- NCIT_C3472 isDefinedBy ncit.owl @default.
- NCIT_C3472 label "Severe Combined Immunodeficiency" @default.
- NCIT_C3472 subClassOf B13f6922888856bf974ed6d65babf8c06 @default.
- NCIT_C3472 subClassOf B774e258ffa9e110a759445b8cc228f6a @default.
- NCIT_C3472 subClassOf NCIT_C27351 @default.
- NCIT_C3472 subClassOf NCIT_C27551 @default.
- NCIT_C3472 subClassOf NCIT_C27871 @default.
- NCIT_C3472 subClassOf NCIT_C28193 @default.
- NCIT_C3472 subClassOf NCIT_C2991 @default.
- NCIT_C3472 subClassOf NCIT_C3101 @default.
- NCIT_C3472 subClassOf NCIT_C3131 @default.
- NCIT_C3472 subClassOf NCIT_C3472 @default.
- NCIT_C3472 subClassOf NCIT_C3507 @default.
- NCIT_C3472 subClassOf NCIT_C7057 @default.