Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
Primary Intraosseous Squamous Cell Carcinoma	EFO_1000492	[A squamous cell carcinoma that arises centrally from the jaw. It derives from odontogenic epithelial remnants. It includes solid type squamous cell carcinoma, squamous cell carcinoma that arises from an odontogenic cyst, and squamous cell carcinoma that derives from a keratocystic odontogenic tumor.]
post-infectious syndrome	MONDO_0021670
Primary Melanocytic Lesion of Meninges	EFO_1000493	[A benign or malignant, circumscribed or diffuse neoplasm that arises from melanocytes in the leptomeninges. It includes diffuse melanocytosis, leptomeningeal melanoma, and melanocytoma.]
Tacaribe virus	NCBITaxon_11631
Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type	EFO_1000490	[An aggressive primary cutaneous B-cell lymphoma, usually involving the lower leg. It is composed of a generally monotonous proliferation of immunoblasts, or less frequently centroblasts, with few admixed reactive cells. This type of lymphoma occurs most often in elderly women who present with rapidly growing tumors, usually on one or both legs. Dissemination to extracutaneous sites is frequent. Treatment with combination chemotherapy is usually required.]
aggressive primary cutaneous B-cell lymphoma	MONDO_0015818
Primary Effusion Lymphoma	EFO_1000491	[Primary effusion lymphoma (PEL) is a large B-cell lymphoma located in the body cavities, characterized by pleural, peritoneal, and pericardial fluid lymphomatous effusions and that is always associated with human herpes virus-8 (HHV-8).]
Epstein-Barr virus-associated malignant lymphoproliferative disorder	MONDO_0017343
human herpesvirus 8-related tumor	MONDO_0015157
tetrasomy 9p	MONDO_0018030	[Tetrasomy 9p is a rare autosomal anomaly characterized by pre- and postnatal growth retardation, psychomotor delay, mild to moderate intellectual disability, hypotonia, microcephaly, dysmorphic features (ocular hypertelorism, low-set, malformed ears, bulbous/beaked nose, microretrognathia, enophthalmos/micropthalmia, epicanthus, strabismus), cleft lip/palate, skeletal abnormalities (hypoplastic nails/distal phalanges, short stature, short neck, contractures), congenital heart defects, renal and urogenital malformations (renal hypoplasia, genital hypoplasia, cryptorchidism).]
syndrome caused by partial chromosomal duplication of the short arm of chromosome 9	MONDO_0700043
post-bacterial disorder	MONDO_0021673
mitochondrial complex 4 deficiency, nuclear type 14	MONDO_0033649
viral disease or post-viral disorder	MONDO_0100321	[A viral infectious disease that result from the presence and activity of a viral agent, or a disorder that follows infection with an viral agent but is distinct from the usual manifestations of the infection itself.]
mitochondrial complex 4 deficiency, nuclear type 12	MONDO_0033646
post-infectious neuralgia	MONDO_0021677
familial acanthosis nigricans	MONDO_0043003	[An instance of acanthosis nigricans (disease) that is caused by an inherited modification of the individual's genome.]
Prostate Rhabdomyosarcoma	EFO_1000498	[A malignant mesenchymal neoplasm with skeletal muscle differentiation affecting the prostate.]
prostate sarcoma	MONDO_0002854	[A rare malignant soft tissue neoplasm that arises from the prostate gland. Representative examples include leiomyosarcoma, rhabdomyosarcoma, and stromal sarcoma.]
rhabdomyosarcoma	EFO_0002918	[A rare aggressive malignant mesenchymal neoplasm arising from skeletal muscle. It usually occurs in children and young adults. Only a small percentage of tumors arise in the skeletal muscle of the extremities. The majority arise in other anatomical sites.]