Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
SKMC	EFO_0002801
SAEC	EFO_0002800	[SAEC is a cell line derived from Small Airway Epithelial Cells]
obsolete_Jurkat	EFO_0002825	[Human T cell leukemia, established from the peripheral blood of a 14-year-old boy with acute lymphoblastic leukemia (ALL) at first relapse in 1976; often this cell line is called "JM (JURKAT and JM are derived from the same patient and are sister clones), occasionally JM may be a subclone with somewhat divergent features.]
HCT116	EFO_0002824	[Human colon carcinoma cell line; established from the primary colon carcinoma of an adult man.]
colorectal cancer cell line	BTO_0001616
LC-1F	EFO_0002827	[A cell line derived from human squamous cell lung carcinoma.]
squamous cell lung carcinoma	EFO_0000708	[A carcinoma arising from squamous bronchial epithelial cells. It may be keratinizing or non-keratinizing. Keratinizing squamous cell carcinoma is characterized by the presence of keratinization, pearl formation, and/or intercellular bridges. Non-keratinizing squamous cell carcinoma is characterized by the absence of keratinization, pearl formation, and intercellular bridges. Cigarette smoking and arsenic exposure are strongly associated with squamous cell lung carcinoma.]
KS-IMM	EFO_0002826	[The tumorigenic KS IMM cell line derives from Kaposi's sarcoma (KS), a highly angiogenic tumor., A KS-IMM is a cell line. A KS-IMM is bearer of a Kaposi's sarcoma.]
MIN6	EFO_0002829	[The murine MIN6 cell line derived from in vivo immortalized insulin-secreting pancreatic beta cells., A MIN6 is a cell line. A MIN6 derives from a mus musculus.]
Lu135	EFO_0002828
small cell lung carcinoma	EFO_0000702	[Small cell lung cancer (SCLC) is a highly aggressive malignant neoplasm, accounting for 10-15% of lung cancer cases, characterized byrapid growth, and early metastasis. SCLC usually manifests as a large hilar mass with bulky mediastinal lymphadenopathy presenting clinically with chest pain, persistent cough, dyspnea, wheezing, hoarseness, hemoptysis, loss of appetite, weight loss, and neurological and endocrine paraneoplastic syndromes. SCLC is primarily reported in elderly people with a history of long-term tobacco exposure.]
Ehlers-Danlos syndrome, vascular-like type	MONDO_0016469	[Ehlers-Danlos, vascular-like type is an adult-onset form of Ehlers-Danlos syndrome characterized by spontaneous dissection of medium-sized arteries during young adulthood, including mainly the iliac, femoral, and renal arteries.]
syndromic agammaglobulinemia	MONDO_0016463	[A agammaglobulinemia that is part of a larger syndrome.]
insulin-resistance syndrome type B	MONDO_0016464	[Type B insulin-resistance syndrome belongs to the group of extreme insulin-resistance syndromes (which includes leprechaunism, the lipodystrophies, Rabson-Mendenhall syndrome, and type A insulin resistance syndrome) and occurs in the context of immune dysfunction.]
polyvalvular heart disease syndrome	MONDO_0016460	[Polyvalvular heart disease syndrome is a recently described syndrome characterized by the combination of polyvalvular heart disease, short stature, facial anomalies and intellectual deficit.]
5q35 microduplication syndrome	MONDO_0016461	[The newly described 5q35 microduplication syndrome is associated with microcephaly, short stature, developmental delay and delayed bone maturation.]
partial trisomy of the long arm of chromosome 5	MONDO_0016956	[Chromosome 5q duplication is a chromosome abnormality that occurs when there is an extra copy of genetic material on the long arm (q) of chromosome 5. The severity of the condition and the signs and symptoms depend on the size and location of the duplication and which genes are involved. Features that often occur in people with chromosome 5q duplication include developmental delay, intellectual disability, behavioral problems and distinctive facial features. Chromosome 5q duplication can be de novo or inherited from a parent with a chromosomal rearrangement such as a balanced translocation. Treatment is based on the signs and symptoms present in each person.]
1-myristoyl-2-palmitoyl-sn-glycero-3-phosphocholine	CHEBI_75062	[A phosphatidylcholine 30:0 in which the phosphatidyl acyl groups at positions 1 and 2 are myristoyl (tetradecanoyl) and palmitoyl (hexadecanoyl) respectively.]
isolated agammaglobulinemia	MONDO_0016462	[Isolated agammaglobulinemia (IA) is the non-syndromic form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by deficient gamma globulins and associated predisposition to frequent and recurrent infections from infancy.]
Speech articulation difficulties	HP_0009088	[Impairment in the physical production of speech sounds.]