Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete failed induction	DOID_10220
vaginal endometrial stromal sarcoma	DOID_5170	[A vagina sarcoma that has_material_basis in endometrial stroma.]
vagina sarcoma	DOID_1901	[A vaginal cancer that has_material_basis in connective tissue.]
pediatric myxoid chondrosarcoma	DOID_6494
arteriolosclerosis	DOID_5162
Monckeberg arteriosclerosis	DOID_5161
adult myxoid chondrosarcoma	DOID_6495	[An adult sarcoma of soft tissue and myxoid chondrosarcoma that is composed_of multiple lobules of chondroblast-like cells, arranged in cords and strands, embedded in a myxoid stroma, and separated by fibrous septa.]
breast epithelioid hemangioma	DOID_6492	[A breast hemangioma that is characterized by islands and cords on hyalinized and myxoid ground substance as well as intracytoplasmic vacuoles that contain typical erythrocytes and are characterized by fusiform or round nucleated cells.]
breast hemangioma	DOID_476	[A breast benign neoplasm that is characterized by a collection of excess blood vessels.]
endometrial stromal tumor	DOID_5166
uterine corpus sarcoma	DOID_5165	[An uterine corpus cancer that is located_in the muscles of the uterus or located_in other tissues that support the uterus.]
extraskeletal myxoid chondrosarcoma	DOID_6496	[An extraosseous chondrosarcoma that has_material_basis_in cells derived from transformed cells that produce cartilage and is characterized by a marked abundance of extracellular mucoid (myxoid) matrix.]
obsolete partial epilepsy, with impairment of consciousness, with intractable epilepsy	DOID_10229
multiple congenital anomalies-hypotonia-seizures syndrome 3	DOID_0080140	[A multiple congenital anomalies-hypotonia-seizures syndrome that is characterized by neonatal hypotonia, lack of psychomotor development, seizures, dysmorphic features, and variable congenital anomalies involving the cardiac, urinary, and gastrointestinal systems and that has_material_basis_in homozygous or compound heterozygous mutation in the PIGT gene on chromosome 20q13.]
multiple congenital anomalies-hypotonia-seizures syndrome	DOID_0080503	[A lipid metabolism disorder that is characterized by phosphatidylinositol glycan anchor biosynthesis class A (PIGA) deficiency.]
ovarian endometrioid stromal sarcoma	DOID_5169	[An ovary sarcoma that arises from endometrial stromal tissue.]
mosaic variegated aneuploidy syndrome 1	DOID_0080141
mosaic variegated aneuploidy syndrome 2	DOID_0080142
congenital fibrosis of the extraocular muscles	DOID_0080143	[An ocular motility disease that is characterized by the inability to move the eyes in certain directions, droopy eyelids and eyes that are fixed in an abnormal position.]
ocular motility disease	DOID_1279