Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Domain and all descendants
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Blood Coagulation Disorders Hemorrhagic and thrombotic disorders that occur as a consequence of abnormalities in blood coagulation due to a variety of factors such as COAGULATIO… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150040 |
| Blood Coagulation Disorders, Inherited Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation. | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150041 |
| Blood Platelet Disorders Disorders caused by abnormalities in platelet count or function. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150075 |
| Blood Protein Disorders Hematologic diseases caused by structural or functional defects of BLOOD PROTEINS. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150083 |
| Bone Marrow Diseases Diseases involving the BONE MARROW. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150096 |
| Bone Marrow Failure Disorders Inherited or acquired diseases characterized by insufficient and/or dysplastic blood cells. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150097 |
| Breast Cancer Lymphedema Abnormal accumulation of lymph in the arm, shoulder and breast area associated with surgical treatment (e.g., MASTECTOMY) or radiation treatment of b… | Pathologic Condition | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150150 |
| Castleman Disease Large benign, hyperplastic lymph nodes. The more common hyaline vascular subtype is characterized by small hyaline vascular follicles and interfollic… | Immune Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150155 |
| Chemotherapy-Induced Febrile Neutropenia FEVER accompanied by a significant reduction in NEUTROPHIL count associated with CHEMOTHERAPY. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150112 |
| Coagulation Protein Disorders Hemorrhagic and thrombotic disorders resulting from abnormalities or deficiencies of coagulation proteins. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150062 |
| Congenital Bone Marrow Failure Syndromes Inherited syndromes characterized by deficiency or absence of various blood cells due to mutations that affect HEMATOPOIETIC STEM CELLS development a… | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150098 |
| Cytopenia A deficiency in or reduction of the number of blood cells. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150107 |
| delta-Thalassemia A hereditary disorder characterized by reduced or absent DELTA-GLOBIN thus effecting the level of HEMOGLOBIN A2, a minor component of adult hemoglobi… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150025 |
| Disseminated Intravascular Coagulation A disorder characterized by procoagulant substances entering the general circulation causing a systemic thrombotic process. The activation of the clo… | Vascular Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150063 |
| Dysgammaglobulinemia An immunologic deficiency state characterized by selective deficiencies of one or more, but not all, classes of immunoglobulins. | Immune Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150085 |
| Dyskeratosis Congenita A predominantly X-linked recessive syndrome characterized by a triad of reticular skin pigmentation, nail dystrophy and leukoplakia of mucous membran… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150099 |
| Ecchymosis Extravasation of blood into the skin, resulting in a nonelevated, rounded or irregular, blue or purplish patch, larger than a petechia. | Pathologic Condition | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150064 |
| Elephantiasis Hypertrophy and thickening of tissues from causes other than filarial infection, the latter being described as ELEPHANTIASIS, FILARIAL. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150151 |
| Elliptocytosis, Hereditary An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape. | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150017 |
| Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150119 |
| Erdheim-Chester Disease A rare form of non-Langerhans-cell histiocytosis (HISTIOCYTOSIS, NON-LANGERHANS-CELL) with onset in middle age. The systemic disease is characterized… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150137 |
| Factor V Deficiency A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency kn… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150046 |
| Factor VII Deficiency An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependen… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150047 |
| Factor X Deficiency Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150048 |
| Factor XI Deficiency A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting i… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150049 |
| Factor XII Deficiency An absence or reduced level of blood coagulation factor XII. It normally occurs in the absence of patient or family history of hemorrhagic disorders … | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150050 |
| Factor XIII Deficiency A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrh… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150051 |
| Fanconi Anemia Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and li… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150007 |
| Favism Hemolytic anemia due to the ingestion of fava beans or after inhalation of pollen from the Vicia fava plant by persons with glucose-6-phosphate dehyd… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150019 |
| Febrile Neutropenia Fever accompanied by a significant reduction in the number of NEUTROPHILS. | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150111 |