All terms in DOID

Label Id Description
high grade glioma DOID_3070 [A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine.]
childhood oligodendroglioma DOID_3183
spinal cord oligodendroglioma DOID_3184
spinal cord glioma DOID_3185 [A spinal cancer that is located in the spinal cord and has_material_basis_in glial cells.]
spinal cancer DOID_5612 [A central nervous system cancer that is located_in the spinal cord. It is mostly formed from metastases from primary cancers elsewhere (commonly breast, prostate, and lung cancer).]
vertebral artery UBERON_0001535
spinal artery UBERON_0002458
adult oligodendroglioma DOID_3186
dextro-looped transposition of the great arteries DOID_0060770 [A congenital heart disease characterized by complete inversion of the great vessels where the aorta incorrectly arises from the right ventricle and the pulmonary artery incorrectly arises from the left ventricle.]
congenital heart disease DOID_1682 [A physical disorder that is characterized by problems with the heart's structure that are present at birth.]
brain oligodendroglioma DOID_3187 [A brain glioma that has_material_basis_in oligodendrocytes.]
brain glioma DOID_0060108 [A brain cancer that has_material_basis_in glial cells.]
obsolete dextro-looped transposition of the great arteries 1 DOID_0060771 [A dextro-looped transposition of the great arteries that has_material_basis_in heterozygous missense mutation in the MED13L gene on chromosome 12q24.]
multiple types of congenital heart defects 6 DOID_0060772 [A congenital heart disease that is characterized by a congenital cardiac malformation characterized by atrioventricular concordance and ventriculoarterial discordance and that has_material_basis_in heterozygous mutation in the GDF1 gene on chromosome 19p13.]
subdivision of oviduct UBERON_0013515
restrictive dermopathy DOID_0060762 [A skin disease characterized by thin, tightly adherent translucent skin with erosions at flexure sites, superficial vessels, typical facial dysmorphism, and generalized joint ankylosis. Prenatal signs may include intrauterine growth retardation, reduced fetal movements, polyhydramnios, and premature rupture of the membranes. Most infants die within the first week of life.]
X-linked juvenile retinoschisis 1 DOID_0060763 [A retinoschisis characterized by schisis (splitting) of the neural retina leading to reduced visual acuity in males due that has_material_basis_in the RS1 gene on chromosome Xp22.]
retinoschisis DOID_8465
autosomal recessive Robinow syndrome DOID_0060764 [A Robinow syndrome characterized by autosomal recessive inheritance of severe skeletal dysplasia characterized by dysmorphic facial features, including frontal bossing, hypertelorism, and broad nose, short-limbed dwarfism, vertebral segmentation, and genital hypoplasia that has_material_basis_in homozygous or compound heterozygous mutations in the ROR2 gene on chromosome 9q22.]
Robinow syndrome DOID_0060254 [A syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities, skeletal malformations and genital abnormalities.]