Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
Crohn's colitis	DOID_0060192	[An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus.]
gastroduodenal Crohn's disease	DOID_0060191	[An inflammatory bowel disease characterized by inflammation located_in stomach and located_in duodenum, has_symptom nausea, has_symptom vomiting, has_symptom weight loss and has_symptom loss of appetite.]
ileocolitis	DOID_0060190	[An inflammatory bowel disease characterized by inflammation located_in colon and located_in ileum, has_symptom diarrhea, has_symptom weight loss, has_symptom abdominal pain in middle or lower right part.]
obsolete Hodgkin's paragranuloma involving intrathoracic lymph nodes	DOID_9067
amyotrophic lateral sclerosis type 7	DOID_0060199	[An amyotrophic lateral sclerosis that has_material_basis_in mutation in loci on chromosome 20.]
amyotrophic lateral sclerosis type 6	DOID_0060198	[An amyotrophic lateral sclerosis that has_material_basis_in mutation in the FUS gene on chromosome 16.]
amyotrophic lateral sclerosis type 5	DOID_0060197	[An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21.]
amyotrophic lateral sclerosis type 4	DOID_0060196	[An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the SETX gene on chromosome 9.]
amyotrophic lateral sclerosis type 3	DOID_0060195	[An amyotrophic lateral sclerosis that has_material_basis_in mutation in loci on chromosome 18.]
amyotrophic lateral sclerosis type 2	DOID_0060194	[An amyotrophic lateral sclerosis that has_material_basis_in mutation in the alsin gene on chromosome 2.]
amyotrophic lateral sclerosis type 1	DOID_0060193	[The most common type of familial ALS that has_material_basis_in mutation in the SOD1 gene on chromosome 21.]
rheumatic congestive heart failure	DOID_14172
obsolete mycosis fungoides involving intrathoracic lymph nodes	DOID_9082
central neurocytoma	DOID_14174
von Hippel-Lindau disease	DOID_14175
macroglobulinemia	DOID_9080
selective IgG deficiency disease	DOID_14176	[A dysgammaglobulinemia that is characterized by isolated deficiency of an IgG subclass, normal total IgG levels, and subsequent increased susceptibility to recurrent infections, atopic disease, and autoimmune conditions.]
anal carcinoma in situ	DOID_9087	[An in situ carcinoma that is located_in the anus.]
congenital hypogammaglobulinemia	DOID_14177
Teleostei	NCBITaxon_32443