All terms in DOID

Label Id Description
vagina sarcoma DOID_1901 [A vaginal cancer that has_material_basis_in connective tissue.]
childhood myxoid chondrosarcoma DOID_6494
arteriolosclerosis DOID_5162 [An arteriosclerosis that is characterized by thickening of the wall of the small arteries and arterioles, caused by deposition of hyaline material in the wall or concentric smooth muscle wall hypertrophy, and results in lumen narrowing and tissue ischemia.]
Monckeberg arteriosclerosis DOID_5161
obsolete 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.]
obsolete 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 severe global developmental delay, hypotonia, and early-onset seizures, associated with multiple cardiac, genitourinary, and gastrointestinal congenital anomalies.]
ovarian endometrioid stromal sarcoma DOID_5169 [An ovary sarcoma that arises from endometrial stromal tissue.]
mosaic variegated aneuploidy syndrome 1 DOID_0080141 [A mosaic variegated aneuploidy syndrome that is characterized by slow growth before and after birth, shorter than average height, unusually small head size, and an increased risk of developing cancer in childhood, and that has_material_basis_in homozygous or compound heterozygous mutation in the BUB1B gene on chromosome 15q15.]
mosaic variegated aneuploidy syndrome 2 DOID_0080142 [A mosaic variegated aneuploidy syndrome that is characterized by slowly before and after birth and typically normal head size and that has_material_basis_in homozygous or compound heterozygous mutation in the CEP57 gene on chromosome 11q21.]
ocular motility disease DOID_1279
hypertensive retinopathy DOID_11561
Cryptococcal meningitis DOID_0080159 [A fungal meningitis that has_material_basis_in Crypococcus fungal infection.]
fungal meningitis DOID_11608 [A meningitis that has_material_basis_in a fungal infection.]