Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
leiomyoma	MONDO_0001572	[A well-circumscribed benign smooth muscle neoplasm characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.]
Mucinous Gastric Adenocarcinoma	EFO_1000386	[A variant of gastric adenocarcinoma with more than half of the tumor containing extracellular mucinous pools.]
gastric adenocarcinoma	EFO_0000503	[A carcinoma that arises from glandular epithelial cells of the stomach]
mucinous carcinoma	EFO_0000197	[An invasive adenocarcinoma composed of malignant glandular cells which contain intracytoplasmic mucin. Often, the infiltrating glandular structures are associated with mucoid stromal formation. It may arise from the large and small intestine, appendix, stomach, lung, ovary, breast, corpus uteri, cervix, vagina, and salivary gland.]
obsolete_mucinuos carcinoma	EFO_1000387
Mixed Tumor of the Salivary Gland	EFO_1000384	[A benign or malignant neoplasm that arises from the salivary glands. It is characterized by the presence of epithelial and mesenchymal elements. This category includes pleomorphic adenoma, carcinoma ex pleomorphic adenoma, and carcinosarcoma., A neoplasm (disease) that involves the saliva-secreting gland.]
salivary gland neoplasm	EFO_0003826	[Tumors of the SALIVARY GLANDS.]
head and neck neoplasia	EFO_0005950	[A benign or malignant neoplasm that affects the anatomic structures of the head and neck region. Representative examples of benign neoplasms include salivary gland pleomorphic adenoma and nasal cavity papilloma. Representative examples of malignant neoplasms include oral cavity squamous cell carcinoma, laryngeal squamous cell carcinoma, and salivary gland carcinoma.]
digestive system neoplasm	EFO_0008549	[A neoplasm (disease) that involves the digestive system.]
Mixed Tumor of the Skin	EFO_1000385	[A rare, benign, slow-growing and painless neoplasm of sweat glands. It usually arises in the head and neck. It is characterized by the presence of a mesenchymal chondroid stroma, fibrosis, and epithelial structures.]
eccrine sweat gland neoplasm	MONDO_0002090	[A neoplasm involving a eccrine sweat gland.]
combined deficiency of factor V and factor VIII	MONDO_0018175	[Combined deficiency of factor V and factor VIII is an inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms.]
intestinal lymphangiectasia	MONDO_0018178	[Dilatation of the intestinal lymphatic system usually caused by an obstruction in the intestinal wall. It may be congenital or acquired and is characterized by diarrhea; hypoproteinemia; peripheral and/or abdominal edema; and protein-losing enteropathies.]
Neuroblastic Tumor	EFO_1000393	[A group of nervous system tumors which display neuronal differentiation. It includes tumors that are composed of immature round cells and tumors that display advanced differentiation and the formation of ganglion cells.]
Neurothekeoma	EFO_1000394	[A benign neoplasm arising from nerve sheaths. It is characterized by the presence of a myxoid stroma.]
nerve sheath neoplasm	MONDO_0002547	[A benign or malignant neoplasm arising from the perineural cells in the sheaths surrounding the nerves. Representative examples include neurofibroma, schwannoma, and malignant peripheral nerve sheath tumor.]
Nasal Cavity Polyp	EFO_1000391	[A soft and painless polypoid mass that arises from the mucosa in the nasal cavity. It is usually the result of an inflammatory process. It may recur following surgical resection.]
nasal cavity disorder	MONDO_0002232	[A disease involving the nasal cavity.]
hereditary glaucoma	MONDO_0018174	[Hereditary glaucoma is a clinically diverse group of rare eye disorders with genetic predisposition characterized by elevated intraocular pressure (IOP) and glaucomatous changes of the optic nerve head, leading to field defects, visual loss and blindness. Hereditary glaucoma can be sub-classified as primary (congenital glaucoma, juvenile glaucoma) or secondary according to the presence or absence of systemic or other ocular anomalies (iridogoniodysgenesis, Stickler syndrome, Coats syndrome). The clinical presentation is variable and is based on age, severity of glaucoma, presence of ocular abnormalities and development of secondary IOP related abnormalities.]
glaucoma	EFO_0000516	[An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed), Increased pressure in the eyeball due to obstruction of the outflow of aqueous humor.]