Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
Decreased circulating globulin level	HP_0032312	[An abnormally reduced concentration of globulins in the blood.]
Increased circulating globulin level	HP_0032311	[An abnormally elevated concentration of globulins in the blood.]
Granulocytosis	HP_0032310	[An increased count of granulocytes in the peripheral blood circulation.]
endothelial cell of artery	CL_1000413	[A blood vessel endothelial cell that is part of an arterial endothelium.]
blood vessel endothelial cell	CL_0000071	[An endothelial cell that lines the vasculature.]
endothelial cell of arteriole	CL_1000412	[An endothelial cell that is part of the arteriole.]
epithelial cell of gall bladder	CL_1000415	[An epithelial cell that is part of the gallbladder.]
endothelial cell of venule	CL_1000414	[An endothelial cell that is part of the venule.]
endothelial cell of vascular tree	CL_0002139	[An endothelial cell of the vascular tree, which includes blood vessels and lymphatic vessels.]
Serinuria	HP_0032349	[A increased concentration of serine in the urine.]
Cutaneous nodular amyloidosis	HP_0032348	[A type of cutaneous amyloidosis that is characterized clinically by waxy, purpuric plaques and nodules and histologically by amyloid deposits in the dermis and subcutaneous tissue.]
Cutaneous macular amyloidosis	HP_0032347	[A type of cutaneous amyloidosis that is characterized by hyperpigmented patches with indefinite margins composed of grayish brown macules, often with a reticulated or rippled appearance. Lesions may present as a hyperpigmented patch composed of small brown macules in a rippled or reticulated pattern.]
Hypoplastic sweat glands	HP_0007387	[Underdevelopment of the sweat glands.]
Aplasia/Hypoplasia of the sweat glands	HP_0011135	[Absence or developmental hypoplasia of the sweat glands.]
Aplasia cutis congenita of scalp	HP_0007385	[A developmental defect resulting in the congenital absence of skin on the scalp.]
Aplasia cutis congenita	HP_0001057	[A developmental defect resulting in the congenital absence of skin in multiple or solitary non-inflammatory, well-demarcated, oval or circular ulcers with a diameter of about 1 to 2 cm. Aplasia cutis congenita most commonly occurs on the scalp, but may present in the face, trunk, or limbs.]
negative regulation of peripheral tolerance induction	GO_0002659	[Any process that stops, prevents, or reduces the frequency, rate, or extent of peripheral tolerance induction.]
negative regulation of tolerance induction dependent upon immune response	GO_0002653	[Any process that stops, prevents, or reduces the frequency, rate, or extent of tolerance induction dependent upon immune response.]
Aberrant melanosome maturation	HP_0007384
Abnormality of dermal melanosomes	HP_0011125	[An abnormality of the melanosomes, i.e., of the cellular organelles in which melanin pigments are synthesized and stored within melanocytes (the cells that produce pigment in the dermis).]