Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Osteomyelitis due to type 2 diabetes mellitus |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Osteomyelitis due to type 1 diabetes mellitus (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Childhood myelodysplastic syndrome (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Osteomyelitis due to type 2 diabetes mellitus |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Osteomyelitis of forefoot (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Gonococcal osteomyelitis (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Osteomyelitis due to type 1 diabetes mellitus (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Percutaneous fine needle aspiration biopsy of bone marrow using imaging guidance (procedure) |
Procedure site - Direct (attribute) |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Percutaneous fine needle aspiration biopsy of bone marrow using imaging guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Transplantation of autologous hematopoietic stem cell (procedure) |
Procedure site - Indirect (attribute) |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic osteomyelitis of femur with draining sinus |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Draining sinus co-occurrent and due to chronic osteomyelitis of forearm (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Draining sinus co-occurrent and due to chronic osteomyelitis of hand (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Draining sinus co-occurrent and due to chronic osteomyelitis of shoulder (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Draining sinus co-occurrent and due to chronic osteomyelitis of ankle and/or foot (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Draining sinus co-occurrent and due to chronic osteomyelitis of humerus (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Chronic osteomyelitis of lower leg with draining sinus |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Draining sinus co-occurrent and due to chronic osteomyelitis of ankle (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Chronic osteomyelitis of foot with draining sinus |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Chronic osteomyelitis |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Acute osteomyelitis of multiple sites |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Osteomyelitis |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Subacute osteomyelitis (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Radiation injury of bone marrow |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Leukaemic reticuloendotheliosis of lymph nodes of head, face and neck |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Diskospondylitis |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Osteomyelitis due to Staphylococcus aureus (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Osteomyelitis of multiple sites |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Acute hematogenous osteomyelitis |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Acute osteomyelitis (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Transplantation of autologous progenitor cell (procedure) |
Procedure site - Indirect (attribute) |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Diffuse sclerosing osteomyelitis |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Q fever osteomyelitis (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Tuberculous osteomyelitis |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Bacterial osteomyelitis |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
SAPHO syndrome |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Chronic osteomyelitis with draining sinus |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
An extremely rare genetic multisystemic disorder with characteristics of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anaemia, which may be accompanied by neutrophilic dermatosis. The disease can be associated with fever, joint pain, delayed bone age, growth failure, short adult stature, and development of flexion contractures. Other reported manifestations include failure to thrive, hepatomegaly, neutropenia, and transient cholestatic jaundice. The clinical course is chronic. Caused by a mutation in LPIN2 (18p11.31), which encodes phosphatidate phosphatase LPIN2 (Lipin-2), important in lipid metabolism. Follows an autosomal recessive pattern of inheritance. |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Brodie's abscess of tibia |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chronic sclerosing nonsuppurative osteomyelitis (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Gonococcal osteomyelitis (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Chronic multifocal osteomyelitis |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Brodie's abscess of coccyx (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Chronic osteomyelitis of multiple sites |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Brodie's abscess |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Brodie's abscess of thoracic spine |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Brodie's abscess of cervical spine (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Brodie's abscess of lumbar spine |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Brodie's abscess of sacrum |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Disorder of central nervous system co-occurrent and due to acute lymphoid leukemia in remission (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Disorder of central nervous system co-occurrent and due to acute lymphoid leukemia |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Aplastic anaemia co-occurrent with human immunodeficiency virus infection |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Philadelphia chromosome-negative precursor B-cell acute lymphoblastic leukaemia |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Aplastic anaemia due to infection |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Parvoviral aplastic crisis |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Aplastic anemia caused by antineoplastic agent |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Edema of bone marrow (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
WT limb blood syndrome (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chronic haematogenous osteomyelitis |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Pasteurella multocida osteomyelitis |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Therapy related acute myeloid leukemia and myelodysplastic syndrome (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Transient abnormal myelopoiesis |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute leukemia of ambiguous lineage (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Aggressive natural killer-cell leukemia (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Myelodysplastic/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Refractory neutropenia |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Refractory thrombocytopenia (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute lymphoid leukemia relapse (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Refractory acute lymphoid leukemia (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hematopoietic subsyndrome of acute radiation syndrome (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Revesz syndrome (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Revesz syndrome (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
B lymphoblastic leukemia lymphoma with t(9:22) (q34;q11.2); BCR-ABL 1 (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute myeloid leukaemia with t(8;16)(p11;p13) translocation |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Myeloid leukemia associated with Down syndrome (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chronic lymphocytic leukemia genetic mutation variant (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Transient abnormal myelopoiesis co-occurrent with Down syndrome (disorder) |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Acute myeloid leukemia with t(6;9)(p23;q34) translocation (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation |
Finding site |
False |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Therapy related acute myeloid leukemia due to and following administration of antineoplastic agent (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) is a rare subtype of acute myeloid leukemia with recurrent cytogenetic abnormalities characterized by clonal proliferation of myeloid blasts with predominantly megakaryoblastic differentiation in the bone marrow and blood, often with extensive infiltration of the abdominal organs. It occurs typically in infants and usually presents with hepatosplenomegaly, anemia, thrombocytopenia and nonspecific symptoms related to ineffective hematopoiesis (fatigue, bleeding and bruising, recurrent infections). Myelofibrosis and fibrosis of other infiltrated organs is also characteristic of this disease. |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Bone marrow cytological material |
Specimen source topography |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Inherited acute myeloid leukemia (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute myeloid leukemia and myelodysplastic syndrome related to radiation (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute myeloid leukaemia and myelodysplastic syndrome related to alkylating agent |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute myeloid leukaemia and myelodysplastic syndrome related to topoisomerase type 2 inhibitor |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Estren-Dameshek anaemia |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Transient hypoplastic anemia |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Constitutional aplastic anaemia |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Constitutional aplastic anemia with malformation |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Fanconi's anemia |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Parvoviral aplastic crisis |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
A rare genetic hematologic disorder characterized by progressive trilineage bone marrow failure (with hypocellularity), developmental delay with learning disabilities and microcephaly. Mild facial dysmorphism and hypotonia have also been reported. There is evidence the disease is caused by homozygous mutation in the ERCC6L2 gene on chromosome 9q22. |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital neutropenia, myelofibrosis, nephromegaly syndrome (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare genetic hematologic disorder characterized by bone marrow failure which manifests with aplastic anemia and/or myelodysplasia, associated with hearing/ear abnormalities (such as deafness, labyrinthitis), inherited in an autosomal dominant manner. Caused by heterozygous mutation in the SRP72 gene on chromosome 4q12. |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Undifferentiated myeloproliferative disease (disorder) |
Finding site |
True |
Bone marrow structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |