All terms in DOID

Label Id Description
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. The most common type of Crohn's disease.]
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 SOD1 gene 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.]
susceptibility to autism 13 MIM_610908
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 [An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS.]
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