Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Iron deficiency anemia secondary to inadequate dietary iron intake (disorder) |
Due to |
False |
Decreased erythrocyte production |
Inferred relationship |
Some |
|
Iron deficiency anaemia due to dietary causes |
Due to |
False |
Decreased erythrocyte production |
Inferred relationship |
Some |
|
Aplastic anemia with AIDS (acquired immunodeficiency syndrome) |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
9 |
Iron deficiency anemia in mother complicating childbirth |
Due to |
False |
Decreased erythrocyte production |
Inferred relationship |
Some |
|
Aplastic anemia caused by antineoplastic agent |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
6 |
Aplastic anaemia co-occurrent with human immunodeficiency virus infection |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
7 |
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) |
Due to |
False |
Decreased erythrocyte production |
Inferred relationship |
Some |
8 |
Congenital dyserythropoietic anemia type IV (CDA IV) is a newly discovered form of CDA characterized by ineffective erythropoiesis and hemolysis that leads to severe anemia at birth. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
5 |
Thrombocytopenia with congenital dyserythropoietic anemia is a rare hematological disorder, seen almost exclusively in males, characterized by moderate to severe thrombocytopenia with hemorrhages with or without the presence of mild to severe anemia. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
1 |
A rare syndromic mitochondrial disease characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
5 |
A rare constitutional aplastic anemia disorder characterized by severe hypo/aplastic anemia or pancytopenia associated with skeletal anomalies (such as radial/ulnar defects and hand/digit abnormalities) and an increased risk of leukemia. There have been no further descriptions in the literature since 1995. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
6 |
A rare acquired aplastic anaemia characterised by a severe normocytic anaemia with normal peripheral leukocyte and platelet counts, reticulocytopenia, high serum ferritin and transferrin saturation levels and isolated, almost complete absence of erythroblasts in the bone marrow with normal granulopoiesis and megakaryopoiesis. It presents with signs of severe anaemia (fatigue, lethargy, pallor, intolerance of physical exercise and exertional dyspnoea) in the absence of haemorrhagic symptoms. |
Due to |
False |
Decreased erythrocyte production |
Inferred relationship |
Some |
8 |
Revesz syndrome is a rare severe phenotypic variant of dyskeratosis congenita with an onset in early childhood, characterized by features of DC (e.g. skin hyper/hypopigmentation, nail dystrophy, oral leukoplakia, high risk of bone marrow failure (BMF) and cancer, developmental delay sparse and fine hair) in conjunction with bilateral exudative retinopathy, and intracranial calcifications. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
10 |
A rare constitutional aplastic anemia 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. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
6 |
Majeed syndrome is a rare genetic multisystemic disorder characterised by chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anaemia, which may be accompanied by neutrophilic dermatosis. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
7 |
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia is a rare, genetic, constitutional dyserythropoietic anemia disorder characterized by moderate to severe anemia without thrombocytopenia, variable degrees of neutropenia, and bone marrow biopsy findings of trilineage dysplasia and hypocellularity of erythroid and granulocytic lineages. Peripheral blood findings include anisocytosis, macrocytosis, poikilocytosis, elliptocytes, and fragmented erythrocytes. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
6 |
Hereditary isolated aplastic anemia is a rare, genetic, constitutional aplastic anemia disorder characterized by severe peripheral blood pancytopenia and bone marrow hypoplasia in multiple individuals of a family, in the absence of any somatic symptoms. Abnormal bleeding, as well as erythrocyte macrocytosis, is reported and patients usually become transfusion dependent. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
7 |
Aase syndrome |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
4 |
Anemia due to disturbance of proliferation AND/OR differentiation of erythroid precursor cells |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
1 |
Fanconi anemia of complementation group C |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
6 |
A rare constitutional aplastic anaemia characterised by aplastic anaemia, intellectual disability, short stature, and microcephaly. Skin pigmentation or cafe au lait spots are often present. Majority of the patients present global developmental delay with impaired motor skills, learning disabilities, speech delay whereas some patients also may have behavioural problems including autistic features. Patients often develop premalignant myelodysplastic syndromes or leukaemia. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Some |
10 |