Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
rheumatic myocarditis	MONDO_0004582	[Inflammation of the myocardium in acute rheumatic heart disease.]
rheumatic heart disease	EFO_1001161	[Cardiac manifestation of systemic rheumatological conditions, such as RHEUMATIC FEVER. Rheumatic heart disease can involve any part the heart, most often the HEART VALVES and the ENDOCARDIUM., An autoinflammatory condition following an infection with Group A Beta Hemolytic Streptococcus (GABHS), in which the heart is attacked by antibodies formed in reaction to a recent GABHS infection. Chief anatomic changes of the valve include leaflet thickening, commissural fusion, and shortening and thickening of the tendinous cords, all of which can result in valvular dysfunction.]
primary cutaneous lymphoma	MONDO_0018898	[Cutaneous lymphoma is a heterogeneous entity with respect to its clinical and pathological features, evolutive profile, prognosis, molecular aetiology and response to therapy. These specifications have been taken into account in recent classifications, which have placed particular importance on the prognostic implications of these different entities.]
embryonic leading edge cell	FBbt_00005746	[Cell at the leading edge of the dorsal epidermis during dorsal closure.]
embryonic dorsal epidermis	FBbt_00005744	[Epidermis of the dorsal region of the embryo.]
characterization of functional areas of human genome	EFO_0002912
embryonic dorsal apodeme	FBbt_00005745	[Dorsal halve of an embryonic apodeme. The discontinuity between dorsal and ventral halves is visible on a lateral view.]
obsolete_rectal carcinoma	EFO_0002915
embryonic anal pad	FBbt_00005748	[Anal pad of the embryo.]
uterine corpus cancer	EFO_0007532	[A malignant neoplasm involving the body of uterus.]
ovarian serous adenocarcinoma	EFO_0002917	[An adenocarcinoma that arises from the ovary and is characterized by the presence of malignant epithelial cells that, in well differentiated tumors, resemble the epithelium of the fallopian tube or, in poorly differentiated tumors, show anaplastic features and marked nuclear atypia.]
malignant ovarian serous tumor	MONDO_0024885	[An invasive malignant neoplasm that arises from the ovary and is characterized by the presence of malignant epithelial cells that, in well differentiated tumors, resemble the epithelium of the fallopian tube or, in poorly differentiated tumors, show anaplastic features and marked nuclear atypia. It includes serous adenocarcinoma and serous adenocarcinofibroma.]
ovary	UBERON_0000992	[The gonad of a female organism which contains germ cells.]
esophageal carcinoma	EFO_0002916	[Esophageal carcinoma (EC) is a tumor arising in the epithelial cells lining the esophagus and can be divided into two subtypes: esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EAC).]
esophageal cancer	MONDO_0007576	[A primary or metastatic malignant neoplasm involving the esophagus.]
esophagus	UBERON_0001043	[Tube that connects the pharynx to the stomach. In mammals, the oesophagus connects the buccal cavity with the stomach. The stratified squamous non-keratinised epithelium lining the buccal cavity is continued through the pharynx down into the oesophagus. The lowest part of the oesophagus (ca. 2 cm) is lined with gastric mucosa and covered by peritoneum. The main body of the oesophagus is lined with small, simple mucous glands. Each gland opens into the lumen by a long duct which pierces the muscularis mucosae (Wilson and Washington, 1989). A sphincter is situated at the point where the oesophagus enters the stomach to prevent gastro-oesophageal reflux, i.e. to prevent acidic gastric contents from reaching stratified epithelia of the oesophagus, where they can cause inflammation and irritation (Wilson and Washington, 1989; Brown et al., 1993).]
dominant hypophosphatemia with nephrolithiasis or osteoporosis	MONDO_0016579
muscular tumor	MONDO_0016123
skeletal muscle cancer	MONDO_0002847	[A malignant neoplasm arising from skeletal muscle.]
hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome	MONDO_0016574	[Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome is a neurocutaneous syndrome characterised by congenital hypomelanotic and hypermelanotic cutaneous macules. It has been described in individuals spanning three generations of an Indian family. Some of the patients also had retarded growth and intellectual deficit.]