All terms in HP

Label Id Description
low-density lipoprotein CHEBI_39026 [A class of lipoproteins of small size (18-25 nm) and low density (1.019-1.063 g/ml) particles with a core composed mainly of cholesterol esters and smaller amounts of triglycerides. The surface monolayer consists mostly of phospholipids, a single copy of apolipoprotein B-100, and free cholesterol molecules. The main function of LDL is to transport cholesterol and cholesterol esters from the liver. Excessive levels are associated with cardiovascular disease.]
Right atrial thrombus HP_0033138 [A thrombus (i.e., a blood clot formed in situ within the vascular system) located in the right atrium of the heart.]
Lymph node abscess HP_0033136 [An inflamed lymph node that is filled with pus.]
Hepatic infarction HP_0033135 [Hepatic infarction is defined as areas of coagulative necrosis from hepatocyte cell death caused by local ischemia. Liver infarctions appear as hypoechoic nonvascular regions on conventional and Doppler sonography.]
Abdominal adhesions HP_0033134 [Fibrous bands (i.e., bands of scar-like tissue) that span two or more intra-abdominal organs and/or the inner abdominal wall (i.e. peritoneal membrane).]
Renal cortical hypoechogeneity HP_0033133
Renal cortical hyperechogenicity HP_0033132 [Increased echogenecity of the kidney cortex.]
Renal medullary hyperechogenicity HP_0033131 [Increased echogenecity of the medullary region of the kidney.]
Delayed ability to crawl HP_0033128 [A failure to achieve the ability to crawl at an appropriate developmental stage. Normal infant motor development is marked by a series of postural milestones including learning to crawl on hands and knees between the ages of 6 and 10 months.]
Insulin insensitivity HP_0008189 [Decreased sensitivity toward insulin.]
Thyroid dysgenesis HP_0008188 [Thyroid dysgenesis is a descriptive term that should be avoided if more precise information is available. However, the HPO keeps retains this term because it is commonly used in the medical literature. In humans, the process of thyroid morphogenesis occurs from the 3rd to 16th week of gestation. Alterations occurring during this period may result in a thyroid gland that is absent (thyroid agenesis or athyreosis), hypoplastic (thyroid hypoplasia), or located in an unusual position (thyroid ectopy). All these entities are grouped under the term thyroid dysgenesis.]
Absence of secondary sex characteristics HP_0008187 [No secondary sexual characteristics are present at puberty.]
Adrenocortical cytomegaly HP_0008186 [The presence of large polyhedral cells with eosinophilic granular cytoplasm and enlarged nuclei in the adrenal cortex.]
Multiple pancreatic beta-cell adenomas HP_0008194 [The presence of multiple pancreatic islet cell adenomas.]
Primary gonadal insufficiency HP_0008193
Thyroid agenesis HP_0008191 [The congenital absence of the thyroid gland.]
Follicular lymphoma HP_0033125 [An indolent B cell lymphoproliferative disorder of transformed follicular center B cells. Follicular lymphoma is characterized by diffuse lymphadenopathy, bone marrow involvement, splenomegaly and less commonly other extranodal sites of involvement.]
Increased serum sorbitol concentration HP_0033124 [An increased level of sorbitol in the blood circulation.]
Elevated circulating osteopontin level HP_0033123 [Abnormally increased level of osteopontin in the blood circulation]
Absent P wave HP_0033122 [The P wave that normally precedes each QRS complex by a fixed PR interval of 120 to 200 milliseconds is not present.]