Terminology Service < Semantic Lookup Platform

All terms in BAO

Label	Id	Description
assay footprint	BAO_0000512	[This describes the physical format such as plate density in which an assay is performed, which is generally a microplate format, but can also be an array format.]
Bloom syndrome	DOID_2717	[An autosomal recessive disease characterized by sun sensitivity, short stature, predisposition to the development of cancer and genomic instability.]
hemopneumothorax	DOID_2718
plasma membrane potential assay	BAO_0002194
JMP syndrome	DOID_0050553	[An autosomal recessive disease that is characterized by childhood onset of joint stiffness and severe contractures of the hands and feet, erythematous skin lesions with subsequent development of severe lipodystrophy.]
nuclear membrane potential assay	BAO_0002195
X-linked sideroblastic anemia with ataxia	DOID_0050554
congenital muscular dystrophy	DOID_0050557	[A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted.]
drug interaction assay	BAO_0002188
infantile onset spinocerebellar ataxia	DOID_0050556
toxicity assay	BAO_0002189
Fukuyama congenital muscular dystrophy	DOID_0050559
Ullrich congenital muscular dystrophy	DOID_0050558
sick building syndrome	DOID_2710	[An extrinsic allergic alveolitis that is characterized by a set of symptoms such as headache, fatigue, eye irritation, and breathing difficulties that affect workers in modern airtight office buildings. The disease is caused by indoor pollutants (as formaldehyde fumes, particulate matter, or microorganisms), and the symptoms tend to disappear when affected individuals leave the building.]
phimosis	DOID_2712
capillary hemangioma	DOID_2725
skin hemangioma	DOID_471
Charcot-Marie-Tooth disease type 3	DOID_0050540
Charcot-Marie-Tooth disease	DOID_10595	[A neuromuscular disease that is characterized by a slowly progressive degeneration of the muscles of the foot, lower leg, hand and forearm.]
dyskeratosis congenita	DOID_2729	[A skin disease characterized by cutaneous pigmentation, premature graying, dystrophy of the nails, leukoplakia of the oral mucosa, continuous lacrimation due to atresia of the lacrimal ducts, often thrombocytopenia, anemia, testicular atrophy in the male carriers and predisposition to cancer.]