Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
retinitis pigmentosa 10	DOID_0110388	[A retinitis pigmentosa that has_material_basis_in mutation in the IMPDH1 gene on chromosome 7q32.]
retinitis pigmentosa 73	DOID_0110389	[A retinitis pigmentosa that has_material_basis_in mutation in the HGSNAT gene on chromosome 8p11.]
retinitis pigmentosa 42	DOID_0110386	[A retinitis pigmentosa that has_material_basis_in mutation in the KLHL7 gene on chromosome 7p15.3.]
Trichomonas tenax trichomoniasis	DOID_0050270	[A trichomoniasis that is caused by a singled-celled protozoan parasite Trichomonas tenax, which is transmitted through oral droplets, by kissing, or on fomites such as eating utensils. Trichomonas tenax causes periodonitis and bronchopulmonary trichomoniasis by aspiration from the oropharynx.]
trichomoniasis	DOID_1947	[A parasitic protozoa infectious disease that is caused by singled-celled protozoan parasites Trichomonas vaginalis or Trichomonas tenax, which infect the urogenital tract and mouth respectively.]
retinitis pigmentosa 9	DOID_0110387	[A retinitis pigmentosa that has_material_basis_in mutation in the RP9 gene on chromosome 7p14.]
necatoriasis	DOID_2790	[A parasitic helminthiasis infectious disease that involves infection of the small intestine of humans, dogs and cats by the nematode Necator americanus causing abdominal pain, diarrhea, cramps, weight loss and anemia. Cutaneous larvae migrans in humans is characterized by skin ruptures and severe itching.]
obsolete hookworm infectious disease	DOID_2791	[A Strongylida infectious disease that involves infection of the small intestine of mammals, cats and dogs by the parasitic nematodes of genus Ancylostoma, Necator and Uncinaria.]
conidiobolomycosis	DOID_0050279	[An subcutaneous mycosis that is a chronic inflammatory or granulomatous fungal infection caused by Conidiobolus species, which is restricted to the nasal submucosa and characterized by polyps or palpable restricted subcutaneous masses. Symptoms include nasal obstruction, drainage and sinus pain. Subcutaneous nodules develop in the nasal and perinasal regions.]
bronchiolitis obliterans	DOID_2799	[A obstructive lung disease involving obstruction of the bronchioles due to inflammation and fibrosis which occurs as a complication of various lung conditions or physiological insults.]
retinitis pigmentosa 61	DOID_0110373	[A retinitis pigmentosa that has_material_basis_in mutation in the CLRN1 gene on chromosome 3q25.]
thelaziasis	DOID_0050261	[A parasitic helminthiasis infectious diseasea that involves infection of the eyes in humans by nematode Thelazia callipaeda causing varying degrees of inflammation and lacrimation. In heavier infections, photophobia, edema, conjunctivitis, and blindness occurs.]
retinitis pigmentosa 68	DOID_0110374	[A retinitis pigmentosa that has_material_basis_in mutation in the SLC7A14 gene on chromosome 3q26.]
dioctophymiasis	DOID_0050260	[A parasitic helminthiasis infectious disease that involves parasitic infection by the nematode Dioctophyme renale in humans after eating undercooked food. The larvae are found in the subcutaneous nodules and kidneys.]
retinitis pigmentosa 56	DOID_0110371	[A retinitis pigmentosa that has_material_basis_in mutation in the IMPG2 gene on chromosome 3q12.3.]
obsolete Pseudocoelomata infectious disease	DOID_0050263	[A parasitic helminthiasis infectious disease that involves infection caused by parasitic invertebrates, which have a pseudocoel. Tissue derived from mesoderm only partly lines the fluid filled body cavity of these animals.]
retinitis pigmentosa 4	DOID_0110372	[A retinitis pigmentosa that has_material_basis_in mutation in the RHO gene on chromosome 3q22.]
obsolete Acoelomata infectious disease	DOID_0050262	[A parasitic helminthiasis infectious disease that involves infection caused by parasitic worms, which are bilaterian, unsegmented, soft-bodied invertebrate animals with no body cavity.]
obsolete tick paralysis	DOID_0050265
retinitis pigmentosa 55	DOID_0110370	[A retinitis pigmentosa that has_material_basis_in mutation in the ARL6 gene on chromosome 3q11.2.]