Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
hypermenorrhea	SYMP_0000854	[Hypermenorrhea is a menorrhagia characterized by an abnormally profuse or prolonged menstrual flow.]
chronic eosinophilic leukemia	DOID_0080367	[A chronic leukemia characterized by a clonal proliferation of eosinophilic precursors resulting in persistently increased numbers of eosinophils in the blood, marrow and peripheral tissues.]
imperforate anus	DOID_10488
obsolete transient disorder of initiating or maintaining wakefulness	DOID_10489
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
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	[Gross hematuria is a hematuria characterized by the production of a visible redness in the urine.]
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 4	DOID_0080360	[A fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the COA6 gene on chromosome 1q42.]
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency	DOID_0050713	[A mitochondrial metabolism disease that has_material_basis_in a deficiency of cytochrome c oxidase.]
anuria	SYMP_0000852	[Anuria is a urinary system symptom characterized by the absence of or defective urine excretion.]
non-invasive bladder papillary urothelial neoplasm	DOID_6239
trimethylaminuria	DOID_0080361	[An inherited metabolic disorder characterized by the inabilty 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.]
spondyloepiphyseal dysplasia tarda	DOID_0080362	[A spondyloepimetaphyseal 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.]