Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C62505> ?p ?o ?g. }
- NCIT_C62505 IAO_0000115 "An autosomal recessive genetic disorder characterized by bone marrow failure, skeletal abnormalities, and an increased incidence of the development of neoplasias." @default.
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- NCIT_C62505 NCIT_NHC0 "C62505" @default.
- NCIT_C62505 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C62505 NCIT_P107 "Fanconi Anemia" @default.
- NCIT_C62505 NCIT_P108 "Fanconi Anemia" @default.
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- NCIT_C62505 NCIT_P325 "A chromosomal instability syndrome that is the most common form of inherited aplastic anemia. It is inherited as an autosomal recessive or X-linked disorder. In addition to bone marrow failure, it is associated with skeletal abnormalities and increased incidence of the development of malignancy. Multiple genes are responsible for Fanconi anemia." @default.
- NCIT_C62505 NCIT_P325 "A rare inherited disorder in which the bone marrow does not make blood cells. It is usually diagnosed in children between 2 and 15 years old. Symptoms include frequent infections, easy bleeding, and extreme tiredness. People with Fanconi anemia may have a small skeleton and brown spots on the skin. They also have an increased risk of developing certain types of cancer." @default.
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- NCIT_C62505 hasExactSynonym "Fanconi Anemia" @default.
- NCIT_C62505 hasExactSynonym "Fanconi's Anemia" @default.
- NCIT_C62505 hasExactSynonym "Fanconi's anemia" @default.
- NCIT_C62505 hasExactSynonym "Pancytopenia, Congenital" @default.
- NCIT_C62505 hasExactSynonym "Panmyelopathy, Fanconi" @default.
- NCIT_C62505 hasExactSynonym "Primary Erythroid Hypoplasia" @default.
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- NCIT_C62505 type Class @default.
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- NCIT_C62505 label "Fanconi Anemia" @default.