Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
erythroid progenitor cell	CL_0000038	[A progenitor cell committed to the erythroid lineage.]
lymphocyte	CL_0000542	[A lymphocyte is a leukocyte commonly found in the blood and lymph that has the characteristics of a large nucleus, a neutral staining cytoplasm, and prominent heterochromatin.]
Decreased serum complement factor B	HP_0005416	[A reduced level of the complement component factor B in circulation.]
Increased alpha-globulin	HP_0005413	[An abnormally increased level of circulationg alpha-globulin. Alpha globulins are a group of serum proteins defined by their mobility on serum electrophoresis. The alpha1-protein fraction is comprised of alpha1-antitrypsin, thyroid-binding globulin, and transcortin. Ceruloplasmin, alpha2-macroglobulin, and haptoglobin contribute to the alpha2-protein band. The alpha2 component is increased as an acute-phase reactant.]
Chronic intestinal candidiasis	HP_0005411	[Persistent overgrowth of Candida albicans in the gastrointestinal tract.]
hematopoietic oligopotent progenitor cell	CL_0002032	[A hematopoietic oligopotent progenitor cell that has the ability to differentiate into limited cell types but lacks lineage cell markers and self renewal capabilities. Cell lacks hematopoeitic lineage markers.]
hematopoietic multipotent progenitor cell	CL_0000837	[A hematopoietic multipotent progenitor cell is multipotent, but not capable of long-term self-renewal. These cells are characterized as lacking lineage cell surface markers and being CD34-positive in both mice and humans.]
malignant cell	CL_0001064	[A neoplastic cell that is capable of entering a surrounding tissue]
neoplastic cell	CL_0001063	[An abnormal cell exhibiting dysregulation of cell proliferation or programmed cell death and capable of forming a neoplasm, an aggregate of cells in the form of a tumor mass or an excess number of abnormal cells (liquid tumor) within an organism.]
abnormal cell	CL_0001061	[A cell found in an organism or derived from an organism exhibiting a phenotype that deviates from the expected phenotype of any native cell type of that organism. Abnormal cells are typically found in disease states or disease models.]
cell	CL_0000000	[A material entity of anatomical origin (part of or deriving from an organism) that has as its parts a maximally connected cell compartment surrounded by a plasma membrane.]
vascular endothelial growth factor receptor 2 (mouse)	PR_P35918	[A vascular endothelial growth factor receptor 2 that is encoded in the genome of mouse.]
vascular endothelial growth factor receptor 2	PR_000002112	[A vascular endothelial growth factor receptor that is a translation product of the human KDR gene or a 1:1 ortholog thereof.]
Decreased T cell activation	HP_0005419	[Decreased or impaired activation of T cells in response to a mitogen, cytokine, chemokine, cellular ligand, or an antigen for which it is specific.]
Abnormal T cell activation	HP_0410035	[Any abnormality in the activation of T cells, i.e. the change in morphology and behavior of a mature or immature T cell resulting from exposure to a mitogen, cytokine, chemokine, cellular ligand, or an antigen for which it is specific.]
Decreased circulating androgen level	HP_0030349	[A reduction in the blood concentration of an androgen, that is, of a steroid hormone that controls development and maintenance of masculine characteristics. The androgens include testosterone and Dehydroepiandrosterone.]
regulation of eating behavior	NBO_0000063
regulation of feeding behavior	NBO_0002436
Depletion of components of the alternative complement pathway	HP_0005389	[An abnormal reduction in the components of the alternative complement pathway, such as the C3 protein or its cleavage products.]
Abnormal circulating luteinizing hormone level	HP_0030345	[An anomaly of the circulating level of luteinizing hormone (LH).]