Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
C-C motif chemokine 27 measurement	EFO_0020198	[The determination of the amount of C-C motif chemokine 27 in a sample]
Krukenberg Tumor	EFO_1000316	[Metastatic signet-ring cell carcinoma to the ovary. The primary site is the gastrointestinal tract or breast.]
metastatic carcinoma	MONDO_0024879	[A carcinoma which has spread from the original site of growth to another anatomic site.]
signet ring cell carcinoma	EFO_0000698	[A usually aggressive, poorly differentiated invasive adenocarcinoma characterized by the presence of malignant glandular cells in which the nucleus is pressed to one side by the presence of intracytoplasmic mucus. It may arise from the stomach, small and large intestine, ampulla of Vater, appendix, gallbladder, pancreas, lung, bladder, breast, and prostate gland.]
C-C motif chemokine 28 measurement	EFO_0020199	[The determination of the amount of C-C motif chemokine 28 in a sample]
brain-specific serine protease 4 measurement	EFO_0020192	[The determination of the amount of brain-specific serine protease 4 in a sample]
corneal dystrophy	MONDO_0018102	[The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise but remains in vogue because of its clinical value.]
brevican core protein measurement	EFO_0020193	[The determination of the amount of brevican core protein in a sample]
Daphnia magna	NCBITaxon_35525
Wolfram syndrome	MONDO_0018105	[Wolfram syndrome (WS) also known as DIDMOAD, is a neurodegenerative disorder characterized by type I diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. Other related problems are urinary tract atony, ataxia, peripheral neuropathy, psychiatric disorders and/or seizures. 2 types of WS may be distinguished: type 1 and type 2 (WS1 and WS2).]
type 1 diabetes mellitus	MONDO_0005147	[A chronic condition characterized by minimal or absent production of insulin by the pancreas.]
brother of CDO measurement	EFO_0020194	[The determination of the amount of brother of CDO in a sample]
C-C motif chemokine 13 measurement	EFO_0020195	[The determination of the amount of C-C motif chemokine 13 in a sample]
Daphnia pulicaria	NCBITaxon_35523
familial primary hypomagnesemia with normocalciuria and normocalcemia	MONDO_0018101	[Familial primary hypomagnesemia with normocalciuria and normocalcemia (FPHNN) is a form of familial primary hypomagnesemia (FPH), characterized by low serum magnesium (Mg) values but inappropriate normal urinary Mg values (i.e. renal hypomagnesemia). The typical symptoms are weakness of the limbs, vertigo, headaches, seizures, brisk tendon reflexes and mild to moderate psychomotor delay.]
familial primary hypomagnesemia with normocalcuria	MONDO_0017626	[Familial primary hypomagnesemia with normocalcuria (FPHN) is a form of familial primary hypomagnesemia (FPH) which is characterized by low magnesium values but normal calcium values in the serum. The disorder consists of three distinct forms which are: autosomal recessive primary hypomagnesemia with normocalcuria and hypocalcemia (ARPHN), familial primary hypomagnesemia with normocalcuria and normocalcemia (FPHNN) and isolated autosomal dominant hypomagnesemia, Glaudemans type.]
bone sialoprotein 2 measurement	EFO_0020190	[The determination of the amount of bone sialoprotein 2 in a sample]
familial primary hypomagnesemia	MONDO_0018100	[A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration.]
disorder of magnesium transport	MONDO_0017765	[An acquired metabolic disease that is has its basis in the disruption of magnesium ion transport.]
brain natriuretic peptide 32 measurement	EFO_0020191	[The determination of the amount of brain natriuretic peptide 32 in a sample]