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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 |
|---|---|---|---|---|
| Thrombocytopenia, Neonatal Alloimmune A condition in newborns caused by immunity of the mother to PLATELET ALLOANTIGENS on the fetal platelets. The PLATELETS, coated with maternal ANTIBOD… | Vascular Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150080 |
| Thrombocytosis Increased numbers of platelets in the peripheral blood. (Dorland, 27th ed) | Vascular Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150082 |
| Thrombophilia A disorder of HEMOSTASIS in which there is a tendency for the occurrence of THROMBOSIS. | Vascular Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150132 |
| Thrombotic Microangiopathies Diseases that result in THROMBOSIS in MICROVASCULATURE. The two most prominent diseases are PURPURA, THROMBOTIC THROMBOCYTOPENIC; and HEMOLYTIC-UREMI… | Vascular Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150081 |
| Thymus Hyperplasia Enlargement of the thymus. A condition described in the late 1940's and 1950's as pathological thymic hypertrophy was status thymolymphaticus and was… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150167 |
| Transfusion Reaction Complications of BLOOD TRANSFUSION. Included adverse reactions are common allergic and febrile reactions; hemolytic (delayed and acute) reactions; an… | Immune Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150133 |
| Tumor Lysis Syndrome A syndrome resulting from cytotoxic therapy, occurring generally in aggressive, rapidly proliferating lymphoproliferative disorders. It is characteri… | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150160 |
| Vaso-Occlusive Crises A common complication of SICKLE CELL DISEASE arises when MICROVESSELS become obstructed by sickled red blood cells, leading to tissue and organ oxyge… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150016 |
| Vitamin K Deficiency A nutritional condition produced by a deficiency of VITAMIN K in the diet, characterized by an increased tendency to hemorrhage (HEMORRHAGIC DISORDER… | Metabolic Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150073 |
| Vitamin K Deficiency Bleeding Hemorrhage caused by vitamin K deficiency. | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150074 |
| von Willebrand Disease, Type 1 A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR. | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150058 |
| von Willebrand Disease, Type 2 A subtype of von Willebrand disease that results from qualitative deficiencies of VON WILLEBRAND FACTOR. The subtype is divided into several variants… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150059 |
| von Willebrand Disease, Type 3 A subtype of von Willebrand disease that results from a total or near total deficiency of VON WILLEBRAND FACTOR. | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150060 |
| von Willebrand Diseases Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as a… | Congenital Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150057 |
| Wandering Spleen A congenital or acquired condition in which the SPLEEN is not in its normal anatomical position but moves about in the ABDOMEN. This is due to laxity… | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150166 |
| Wiskott-Aldrich Syndrome A rare, X-linked immunodeficiency syndrome characterized by ECZEMA; LYMPHOPENIA; and, recurrent pyogenic infection. It is seen exclusively in young b… | Syndrome | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150061 |
| Xanthogranuloma, Juvenile Benign disorder of infants and children caused by proliferation of HISTIOCYTES, macrophages found in tissues. These histiocytes, usually lipid-laden … | Disorder | Pathology | Hematopoietic System [curated_secondary] | AMW:DIS:150140 |