All terms in HP

Label Id Description
Acute promyelocytic leukemia HP_0004836 [A type of acute myeloid leukemia in which abnormal promyelocytes predominate.]
Acute monocytic leukemia HP_0004845 [The accumulation of transformed primitive hematopoietic blast cells, which lose their ability of normal differentiation and proliferation.]
Prolonged bleeding after surgery HP_0004846 [Bleeding that persists longer than the normal time following a surgical procedure.]
Prolonged bleeding following procedure HP_0011890 [Prolonged or protracted bleeding following an invasive procedure or intervention.]
Coombs-positive hemolytic anemia HP_0004844 [A type of hemolytic anemia in which the Coombs test is positive.]
Reduced factor XII activity HP_0004841 [Decreased activity of coagulation factor XII. Factor XII (fXII) is part of the intrinsic coagulation pathway and binds to exposed collagen at site of vessel wall injury, activated by high-MW kininogen and kallikrein, thereby initiating the coagulation cascade.]
Abnormality of the intrinsic pathway HP_0010989 [An abnormality of the intrinsic pathway (also known as the contact activation pathway) of the coagulation cascade.]
Hypochromic microcytic anemia HP_0004840 [A type of anemia characterized by an abnormally low concentration of hemoglobin in the erythrocytes and lower than normal size of the erythrocytes.]
Hypochromic anemia HP_0001931 [A type of anemia characterized by an abnormally low concentration of hemoglobin in the erythrocytes.]
wall of gallbladder UBERON_0036343
abdominal wall UBERON_0003697 [The tissues that surround the organs that are present within the abdominal cavity. The abdominal wall tissue is composed of layers of fat, parietal peritoneum, fascia, and muscles.]
Ph-positive acute lymphoblastic leukemia HP_0004848 [A subset of acute lymphoblastic leukemia that results from a reciprocal translocation between the ABL-1 oncogene and a breakpoint cluster region (BCR), resulting in a fusion gene, BCR-ABL, that encodes an oncogenic protein with constitutively active tyrosine kinase activity.]
Horner syndrome HP_0002277 [An abnormality resulting from a lesion of the sympathetic nervous system characterized by a combination of unilateral ptosis, miosis, and often ipsilateral hypohidrosis and conjunctival injection.]
Abnormal autonomic nervous system physiology HP_0012332 [A functional abnormality of the autonomic nervous system.]
Miosis HP_0000616 [Abnormal (non-physiological) constriction of the pupil.]
Ptosis HP_0000508 [The upper eyelid margin is positioned 3 mm or more lower than usual and covers the superior portion of the iris (objective); or, the upper lid margin obscures at least part of the pupil (subjective).]
Tetraparesis HP_0002273 [Weakness of all four limbs.]
Tetraplegia/tetraparesis HP_0030182 [Loss of strength in all four limbs. Tetraplegia refers to a complete loss of strength, whereas Tetraparesis refers to an incomplete loss of strength.]
Poor motor coordination HP_0002275
obsolete Autonomic dysregulation HP_0002271