Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
laryngeal small cell carcinoma	DOID_7144
localized scleroderma	DOID_8472
scleroderma	DOID_419	[A rheumatic disease and collagen disease that involves the abnormal growth of connective tissue, which supports the skin and internal organs.]
prostate small cell carcinoma	DOID_7141
thymus small cell carcinoma	DOID_7142
obsolete staphylococcal pneumonia	DOID_12608	[A staphylococcal infectious disease that is caused due to the infection by Gram-positive bacterium Staphylococcus aureus, which is an important cause of hospital-acquired infection that results in the formation of abscesses, empyema, pneumothorax, and cyst.]
actinomycosis	DOID_8478	[A commensal bacterial infectious disease that results in infection, which is characterized by contiguous spread, suppurative and granulomatous inflammation, and formation of multiple abscesses and sinus tracts that may discharge sulfur granules, has_material_basis_in Actinomyces israelii, has_material_basis_in Actinomyces gerencseriae, has_material_basis_in Actinomyces naeslundii, has_material_basis_in Actinomyces odontolyticus, has_material_basis_in Actinomyces viscosus, has_material_basis_in Actinomyces meyeri, has_material_basis_in Propionibacterium propionicum, which require a break in the integrity of the mucous membranes and the presence of devitalized tissue to invade deeper body structures.]
amenorrhea	DOID_13938	[A female reproductive system disease that is characterized by the absence of menstruation.]
rheumatoid arthritis	DOID_7148	[An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint.]
Whipple disease	DOID_8476
obsolete papillary cystic tumor	DOID_7145
obsolete metastasis to adrenals	DOID_12605
hypertrophic cardiomyopathy 25	DOID_0110328	[A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TCAP gene on chromosome 17q12.]
ectodermal dysplasia 6	DOID_0111659	[A pure hair and nail ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 17p12-q21.2.]
Langerhans cell sarcoma	DOID_7146	[A histiocytic and dendritic cell cancer that derives from the lymph nodes, derives from the skin, derives from the liver, derives from the spleen and derives from bones.]
Langerhans cell	CL_0000453
obsolete malabsorption syndrome	DOID_8477
obsolete secondary malignant neoplasm of suprarenal gland	DOID_12604
Leber congenital amaurosis 6	DOID_0110329	[A Leber congenital amaurosis that is characterized by early photophobia, hypermetropia less than +7 diopters, and visual acuity in the range of 20/400 to count fingers and has_material_basis_in mutation in the RPGRIP1 gene on chromosome 14q11.]
obsolete metastatic parathyroid cancer	DOID_7149