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 |
Existential restriction modifier (core metadata concept) |
|
Iron deficiency anemia due to dietary causes (disorder) |
Due to |
False |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Aplastic anemia with AIDS (acquired immunodeficiency syndrome) |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
9 |
Iron deficiency anemia in mother complicating childbirth |
Due to |
False |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Aplastic anemia caused by antineoplastic agent |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Aplastic anaemia co-occurrent with human immunodeficiency virus infection |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) |
Due to |
False |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Congenital dyserythropoietic anemia type IV (disorder) |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder) |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
WT limb blood syndrome (disorder) |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Adult pure red cell aplasia (disorder) |
Due to |
False |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Revesz syndrome (disorder) |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
10 |
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. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
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. |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Hereditary isolated aplastic anemia |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Aase syndrome |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Anemia due to disturbance of proliferation AND/OR differentiation of erythroid precursor cells (disorder) |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fanconi anemia of complementation group C |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Aplastic anemia, intellectual disability, dwarfism syndrome (disorder) |
Due to |
True |
Decreased erythrocyte production |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
10 |