All terms in DOID

Label Id Description
Hirschsprung's disease DOID_10487 [A megacolon that is characterized by a blockage of the large intestine due to improper muscle movement in the bowel.]
esophageal atresia DOID_10485
childhood teratoma of the ovary DOID_6230 [An ovarian germ cell teratoma that presents in childhood.]
ovarian germ cell teratoma DOID_5567
psoriasis DOID_8893 [A skin disease that is characterized by patches of thick red skin and silvery scales.]
pityriasis rosea DOID_8892 [A dermatitis that is characterized by an initial large round spot on the chest, abdomen, or back, often referred to as a herald patch, that is usually followed within a week by a distinctive pattern of similar but smaller papules on the torso, arms, and legs.]
ovarian biphasic or triphasic teratoma DOID_6232 [An ovarian germ cell teratoma that is composed of tissues that originate from two or three of the following germ layers, endoderm, ectoderm, or mesoderm.]
vulvar eccrine porocarcinoma DOID_7565 [A vulva carcinoma that is characterized by heterogenous histology that includes squamous cells, mucinous cells, clear cells, pigmented cells, and spindle cells and derives_from eccrine sweat glands.]
eccrine porocarcinoma DOID_7566
gross hematuria SYMP_0000851 [A hematuria that is characterized by the production of a visible redness in the urine.]
mitochondrial complex IV deficiency nuclear type 13 DOID_0080360 [A COX deficiency, infantile mitochondrial myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the COA6 gene on chromosome 1q42.]
COX deficiency, infantile mitochondrial myopathy DOID_0050713 [A cytochrome-c oxidase deficiency disease characterized by myotonia, abnormalities of the heart and kidneys, and lactic acidosis.]
anuria SYMP_0000852 [A urinary system symptom that is characterized by the absence of, or by defective, urine excretion.]
non-invasive bladder papillary urothelial neoplasm DOID_6239
trimethylaminuria DOID_0080361 [An inherited metabolic disorder characterized by the inability to break down trimethylamine and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding flavin-containing monooxygenase-3 on chromosome 1q24.]
vulvar clear cell hidradenocarcinoma DOID_7567 [A vulva carcinoma that derives_from sweat glands and is characterized by the presence of clear cells.]
X-linked spondyloepiphyseal dysplasia tarda DOID_0080362 [A spondyloepiphyseal dysplasia that is characterized by impaired growth of bones of the spine and the ends of long bones in the arms and legs and has_material_basis_in mutation in the SEDL gene on chromosome Xp22.]
spondyloepiphyseal dysplasia tarda DOID_0112284 [A spondyloepiphyseal dysplasia characterized by impaired growth of the bones of the spine and the ends of the long bones that becomes apparent in after birth.]
congested sclera SYMP_0000850 [Congested sclera is a hyperemia characterized as the congestion of the vessels of the outer layer of the eye containing collagen and elastic fibers.]
obsolete adult brain meningioma DOID_7568