All terms in DOID

Label Id Description
obsolete influenza myositis DOID_0050164
cataract 40 DOID_0110272 [A cataract that has_material_basis_in mutation in the NHS gene on chromosome Xp22.]
obsolete influenza myocarditis DOID_0050163
tuberculous salpingitis DOID_0050166 [An urogenital tuberculosis that results_in formation of granulomas located_in fallopian tube.]
cataract 17 multiple types DOID_0110270 [A cataract that has_material_basis_in heterozygous or homozygous mutation in the beta-B1 crystallin gene (CRYBB1) on chromosome 22q12.]
obsolete tuberculous mesenteric gland DOID_0050165 [A tuberculosis that involves infection of the mesenteric glands by tuberculosis causing mycobacteria. The symptoms include distended abdomen, persistent intestinal indigestion, diarrhea, flatulence, and abdominal pain.]
cataract 23 DOID_0110271 [A cataract that has_material_basis_in heterozygous mutation in the crystallin beta-A4 gene (CRYBA4) on chromosome 22q12.]
autoimmune polyendocrine syndrome type 2 DOID_0050168 [An autoimmune polyendocrine syndrome that is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. It is more heterogeneous and has not been linked to one gene.]
autoimmune polyendocrine syndrome DOID_14040 [An autoimmune disease of endocrine system characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs.]
autoimmune polyendocrine syndrome type 1 DOID_0050167 [An autoimmune polyendocrine syndrome that is inherited in an autosomal recessive fashion, which is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs.]
autosomal recessive limb-girdle muscular dystrophy type 2D DOID_0110278 [An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the alpha-sarcoglycan gene (SGCA) on chromosome 17q.]
autosomal recessive limb-girdle muscular dystrophy type 2E DOID_0110279 [An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding beta-sarcoglycan (SGCB) on chromosome 4q12.]
inhalation anthrax DOID_0050160 [An anthrax disease that results in infection located in lung lymph nodes brought on by breathing in the spores of the bacteria Bacillus anthracis. The first symptoms of inhalation anthrax are like cold or flu symptoms and can include a sore throat, mild fever and muscle aches. Later symptoms include cough, chest discomfort, shortness of breath, tiredness and muscle aches.]
autosomal recessive limb-girdle muscular dystrophy type 2B DOID_0110276 [An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the skeletal muscle protein dysferlin (DYSF) on chromosome 2p13.]
autosomal recessive limb-girdle muscular dystrophy type 2C DOID_0110277 [An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12.]
cutaneous lupus erythematosus DOID_0050169 [A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight.]
childhood epithelioid sarcoma DOID_7095
columnar cell papillary thyroid carcinoma DOID_7088 [A papillary thyroid carcinoma that is characterized by the presence of pseudostratified malignant follicular cells.]
tall cell papillary thyroid carcinoma DOID_7089 [A papillary thyroid carcinoma that is characterized by the presence of tall malignant follicular cells, arranged in papillary and trabecular patterns.]
multicentric papillary thyroid carcinoma DOID_7086 [A papillary thyroid carcinoma arising in the thyroid gland from multiple foci.]