Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete Reoviridae infectious disease	DOID_1334	[A dsRNA virus infectious disease that results_in infection in animals and humans, has_material_basis_in Reoviridae viruses.]
Abnormality of body weight	HP_0004323	[An abnormal increase or decrease of weight or an abnormal distribution of mass in the body.]
obsolete african horse sickness	DOID_1333	[A viral infectious disease that results_in infection in horses, mules, donkeys and zebras located_in lung, has_material_basis_in African horsesickness virus, which is transmitted_by biting midge, Culicoides imicola, transmitted_by Culex mosquito, transmitted_by Anopheles mosquito, transmitted_by Aedes mosquito, transmitted_by Hyalomma tick, and transmitted_by Rhipicephalus tick. The infection has_symptom tachypnea, has_symptom forced expiration, has_symptom profuse sweating, has_symptom spasmodic coughing, and has_symptom ecchymoses on the tongue.]
obsolete Bunyaviridae infectious disease	DOID_1332	[A (-)ssRNA virus infectious disease that results_in infection in rodents and humans, has_material_basis_in Bunyaviridae viruses, which are transmitted_by arthropod vectors.]
myoepithelioma	DOID_2661	[A sweat gland neoplasm that is composed_of outgrowths of myoepithelial cells from a sweat gland.]
Nematocera	NCBITaxon_7148
obsolete urinary tract infiltrating transitional cell carcinoma	DOID_3997
obsolete benign mesenchymoma	DOID_2667
Bartholin's gland transitional cell carcinoma	DOID_3998	[A Bartholin's gland carcinoma that derives_from transitional epithelial cells.]
Diamond-Blackfan anemia	DOID_1339	[A congenital hypoplastic anemia that is characterized by anemia (low red blood cell counts) with decreased erythroid progenitors in the bone marrow and has_material_basis_insufficient levels of red blood cells due to bone marrow dysfunction.]
Donohue syndrome	DOID_0050470	[A syndrome that is characterized by protuberant and low-set ears, flaring nostrils, thick lips, enlarged secondary sex organs and overwhelming insulin resistance and has_material_basis_in mutation within the INSR gene causing abnormalities in the insulin receptor.]
ovarian Brenner tumor	DOID_2636	[An ovarian benign neoplasm that has_material_basis_in the surface epithelium of the ovary.]
papillary follicular thyroid adenocarcinoma	DOID_3968
monilethrix	DOID_0050472	[A hair disease that is characterized by short, easily broken hair that results in alopecia and has_material_basis_in mutations in genes for type II hair cortex keratins.]
Carney complex	DOID_0050471	[A syndrome characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity.]
breast pericanalicular fibroadenoma	DOID_2639	[A breast fibroadenoma that is characterized by stromal proliferation around epithelial structures.]
obsolete RNA virus infectious disease	DOID_1301	[A viral infectious disease that results_in infection, has_material_basis_in RNA viruses, which have RNA as their genetic material.]
Netherton syndrome	DOID_0050474	[A skin disease that is characterized by chronic skin inflammation, trichorrhexis invaginata, atopic dermatitis and has_material_basis_in mutations in the SPINK5 gene resulting in reduced capacity to inhibit serine proteases expressed in the skin.]
Alstrom syndrome	DOID_0050473	[A syndrome that is characterized by multiorgan dysfunction. The key features are childhood obesity, blindness due to congenital retinal dystrophy, and sensorineural hearing loss with autosomal recessive inheritance and has_material_basis_in mutations in the ALMS1 gene.]
Barth syndrome	DOID_0050476	[A lipid metabolism disorder that has_material_basis_in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin.]