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- NCIT_C61236 IAO_0000115 "An inherited condition characterized by aplasia of the erythroid series only. The white cells and platelets are not affected. Patients develop anemia usually in infancy." @default.
- NCIT_C61236 NCIT_A13 NCIT_C107652 @default.
- NCIT_C61236 NCIT_A13 NCIT_C177126 @default.
- NCIT_C61236 NCIT_A13 NCIT_C177129 @default.
- NCIT_C61236 NCIT_A13 NCIT_C177132 @default.
- NCIT_C61236 NCIT_A13 NCIT_C177135 @default.
- NCIT_C61236 NCIT_A13 NCIT_C177138 @default.
- NCIT_C61236 NCIT_A13 NCIT_C177141 @default.
- NCIT_C61236 NCIT_A13 NCIT_C177144 @default.
- NCIT_C61236 NCIT_A13 NCIT_C177154 @default.
- NCIT_C61236 NCIT_A13 NCIT_C21396 @default.
- NCIT_C61236 NCIT_A13 NCIT_C24750 @default.
- NCIT_C61236 NCIT_NHC0 "C61236" @default.
- NCIT_C61236 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C61236 NCIT_P107 "Congenital Pure Red Cell Aplasia" @default.
- NCIT_C61236 NCIT_P108 "Congenital Pure Red Cell Aplasia" @default.
- NCIT_C61236 NCIT_P207 "C0949116" @default.
- NCIT_C61236 NCIT_P322 "CCPS" @default.
- NCIT_C61236 NCIT_P322 "CTRP" @default.
- NCIT_C61236 NCIT_P322 "Cellosaurus" @default.
- NCIT_C61236 NCIT_P322 "NICHD" @default.
- NCIT_C61236 NCIT_P322 "PCDC" @default.
- NCIT_C61236 NCIT_P325 "A very rare disorder in which the bone marrow doesn't make enough red blood cells. It is usually seen in the first year of life. Patients may have deformed thumbs and other physical problems. They also have an increased risk of leukemia and sarcoma, especially osteosarcoma (bone cancer). Patients with congenital pure red cell aplasia may have a mutation (change) in one of the genes that make proteins found in the cell's ribosomes." @default.
- NCIT_C61236 NCIT_P325 "An inherited condition characterized by aplasia of the erythroid series only. The leukocytes and platelets are not affected. Patients develop anemia, usually in infancy." @default.
- NCIT_C61236 NCIT_P366 "Diamond-Blackfan_Anemia" @default.
- NCIT_C61236 NCIT_R100 NCIT_C12219 @default.
- NCIT_C61236 NCIT_R100 NCIT_C12431 @default.
- NCIT_C61236 NCIT_R100 NCIT_C12919 @default.
- NCIT_C61236 NCIT_R100 NCIT_C13018 @default.
- NCIT_C61236 NCIT_R100 NCIT_C41165 @default.
- NCIT_C61236 NCIT_R101 NCIT_C12219 @default.
- NCIT_C61236 NCIT_R101 NCIT_C12919 @default.
- NCIT_C61236 NCIT_R101 NCIT_C41165 @default.
- NCIT_C61236 NCIT_R103 NCIT_C12219 @default.
- NCIT_C61236 NCIT_R103 NCIT_C12801 @default.
- NCIT_C61236 NCIT_R103 NCIT_C41168 @default.
- NCIT_C61236 NCIT_R104 NCIT_C12219 @default.
- NCIT_C61236 NCIT_R104 NCIT_C12508 @default.
- NCIT_C61236 NCIT_R104 NCIT_C21599 @default.
- NCIT_C61236 NCIT_R104 NCIT_C32725 @default.
- NCIT_C61236 NCIT_R108 NCIT_C3367 @default.
- NCIT_C61236 NCIT_R108 NCIT_C3824 @default.
- NCIT_C61236 NCIT_R108 NCIT_C54062 @default.
- NCIT_C61236 NCIT_R108 NCIT_C7057 @default.
- NCIT_C61236 normalizedInformationContent "84.132738204908478" @default.
- NCIT_C61236 referenceCount "11" @default.
- NCIT_C61236 hasExactSynonym "Blackfan-Diamond anemia" @default.
- NCIT_C61236 hasExactSynonym "Congenital Pure Red Cell Aplasia" @default.
- NCIT_C61236 hasExactSynonym "DBA" @default.
- NCIT_C61236 hasExactSynonym "Diamond Blackfan" @default.
- NCIT_C61236 hasExactSynonym "Diamond-Blackfan Anemia" @default.
- NCIT_C61236 hasExactSynonym "Diamond-Blackfan anemia" @default.
- NCIT_C61236 hasExactSynonym "congenital hypoplastic anemia" @default.
- NCIT_C61236 hasExactSynonym "congenital pure red cell aplasia" @default.
- NCIT_C61236 hasExactSynonym "erythrogenesis imperfecta" @default.
- NCIT_C61236 hasExactSynonym "inherited erythroblastopenia" @default.
- NCIT_C61236 inSubset NCIT_C116977 @default.
- NCIT_C61236 inSubset NCIT_C118168 @default.
- NCIT_C61236 inSubset NCIT_C132009 @default.
- NCIT_C61236 inSubset NCIT_C165258 @default.
- NCIT_C61236 inSubset NCIT_C177281 @default.
- NCIT_C61236 inSubset NCIT_C177516 @default.
- NCIT_C61236 inSubset NCIT_C179478 @default.
- NCIT_C61236 inSubset NCIT_C179491 @default.
- NCIT_C61236 inSubset NCIT_C192842 @default.
- NCIT_C61236 inSubset NCIT_C90259 @default.
- NCIT_C61236 type Class @default.
- NCIT_C61236 isDefinedBy ncit.owl @default.
- NCIT_C61236 label "Congenital Pure Red Cell Aplasia" @default.
- NCIT_C61236 subClassOf NCIT_C104003 @default.
- NCIT_C61236 subClassOf NCIT_C165614 @default.
- NCIT_C61236 subClassOf NCIT_C26323 @default.
- NCIT_C61236 subClassOf NCIT_C26324 @default.
- NCIT_C61236 subClassOf NCIT_C27551 @default.
- NCIT_C61236 subClassOf NCIT_C28193 @default.
- NCIT_C61236 subClassOf NCIT_C2991 @default.
- NCIT_C61236 subClassOf NCIT_C3101 @default.
- NCIT_C61236 subClassOf NCIT_C3266 @default.
- NCIT_C61236 subClassOf NCIT_C34433 @default.
- NCIT_C61236 subClassOf NCIT_C34974 @default.
- NCIT_C61236 subClassOf NCIT_C35814 @default.
- NCIT_C61236 subClassOf NCIT_C53529 @default.
- NCIT_C61236 subClassOf NCIT_C53531 @default.
- NCIT_C61236 subClassOf NCIT_C54705 @default.
- NCIT_C61236 subClassOf NCIT_C61236 @default.
- NCIT_C61236 subClassOf NCIT_C7057 @default.
- NCIT_C61236 subClassOf NCIT_C80693 @default.
- NCIT_C61236 subClassOf NCIT_C94810 @default.