Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
angioedema	DOID_1558	[A skin disease characterized by the rapid swelling of the dermis, subcutaneous tissue, mucosa and submucosal tissues.]
craniofrontonasal syndrome	DOID_14737	[A syndrome that has_material_basis_in mutation in the EFNB1 gene on chromosome Xq13 and is characterized in hemizygous males by hypertelorism and with greater severity in females by frontonasal dysplasia, craniofacial asymmetry, craniosynostosis, bifid nasal tip, grooved nails, wiry hair, and abnormalities of the thoracic skeleton.]
pulmonary sarcoidosis	DOID_13406	[A sarcoidosis that is characterized by noncaseating granulomatous infiltration of the lungs and supporting lymph nodes, bilateral hilar adenopathy, and pulmonary issues, has_symptom shortness of breath, fatigue, wheezing, and chronic cough, and develops_from a type IV hypersensitivity reaction.]
cardiac sarcoidosis	DOID_13405	[A sarcoidosis that is characterized by conduction abnormalities, arrhythmias, and congestive heart failure with noncaseating granulomas present on endomyocardial biopsy, and develops_from a type IV hypersensitivity reaction with noncaseating granulomas infiltrating the myocardial tissue, especially that of the left ventricle.]
uveoparotid fever	DOID_13404	[A sarcoidosis that is characterized by unilateral facial nerve palsy, parotid gland enlargement, anterior uveitis, and low grade fever, and develops_from a type IV hypersensitivity reaction with noncaseating granulomatous infiltration of especially the parotid glands which compresses the facial nerve.]
neurosarcoidosis	DOID_13403	[A sarcoidosis that is characterized by involvement of the nervous symptom with cranial nerve palsy, diffuse meningeal disease, acute polyneuropathy, myelitis, or hypothalamic pituitary axis malformation, develops_from a type IV hypersensitivity reaction with noncaseating granulomas involving the nervous system.]
skin sarcoidosis	DOID_13402
angioid streaks	DOID_13401
Klebsiella granulomatis	NCBITaxon_39824
Klebsiella	NCBITaxon_570
perforation of bile duct	DOID_13409
obsolete metastasis to pleura	DOID_13408
hypercalcemic sarcoidosis	DOID_13407
obsolete progressive high-tone neural deafness	DOID_14739
trichorhinophalangeal syndrome type I	DOID_14743	[A syndrome that is characterized by short stature, sparse hair, a bulbous nasal tip and cone-shaped epiphyses (the growing ends of bones), as well as severe generalized shortening of all finger and toe bones (brachydactyly).]
Partington syndrome	DOID_14744	[A syndrome characterized by intellectual disability, focal dystonia of the hands and dysarthria.]
Sotos syndrome	DOID_14748	[A syndrome that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life.]
alexia	DOID_13417	[An agnosia that is a loss of the ability to recognize text.]
obsolete diabetes mellitus insulin dependent type, not stated as uncontrolled, with peripheral circulatory disorder	DOID_13416
hepatic encephalopathy	DOID_13413	[A brain disease that is characterized by loss of brain function, the occurrence of confusion, altered level of consciousness, and coma that results when the liver is unable to remove toxins from the blood.]