All terms in DOID

Label Id Description
obsolete Trichophyton soudanense tinea capitis DOID_0050106 [An endothrix infectious disease that results_in anthropophilic fungal infection located_in scalp and located_in hair, has_material_basis_in Trichophyton soudanense.]
endothrix infectious disease DOID_0050105 [A tinea capitis that results_in fungal infection located_in hair, has_material_basis_in Ascomycota fungi that belong to a group called dermatophytes, which produce arthroconidia within the hair shaft only.]
obsolete Trichophyton violaceum tinea capitis DOID_0050108 [An endothrix infectious disease that results_in anthropophilic fungal infection located_in skin, located_in nail, located_in beard, and located_in scalp, has_material_basis_in Trichophyton violaceum and results_in_formation_of scaling lesions. The hairs become notably fragile and break easily at the level of the scalp. The rest of the infected follicle looks like black dots.]
obsolete Trichophyton tonsurans tinea capitis DOID_0050107 [An endothrix infectious disease that results_in anthropophilic fungal infection located_in skin, located_in nail and located_in scalp, has_material_basis_in Trichophyton tonsurans and results_in_formation_of scaling lesions.]
motility-related diarrhea DOID_0050131 [A diarrhea which is caused by the rapid movement of food through the intestines (hypermotility). If the food moves too quickly through the GI tract, there is not enough time for sufficient nutrients and water to be absorbed.]
osmotic diarrhea DOID_0050130 [A dirrhea that occurs when too much water is drawn into the bowels. This can be the result of maldigestion (e.g., pancreatic disease or Coeliac disease), in which the nutrients are left in the lumen to pull in water. Osmotic diarrhea can also be caused by osmotic laxatives (which work to alleviate constipation by drawing water into the bowels). In healthy individuals, too much magnesium or vitamin C or undigested lactose can produce osmotic diarrhea and distention of the bowel. A person who does not have lactose intolerance can have difficulty absorbing lactose after an extraordinarily high intake of dairy products.]
inflammatory diarrhea DOID_0050132 [A gastrointestinal system infectious disease involving diarrhea that occurs when there is damage to the mucosal lining or brush border, which leads to a passive loss of protein-rich fluids, and a decreased ability to absorb these lost fluids. It can be caused by bacterial infections, viral infections, parasitic infections, or autoimmune problems such as inflammatory bowel diseases. It can also be caused by tuberculosis, colon cancer, and enteritis.]
subcutaneous mycosis DOID_0050135 [A fungal infectious disease that results_in infection located_in skin or located_in subcutaneous tissue, has_material_basis_in Fungi, which penetrate the dermis or even deeper during or after a skin trauma.]
autosomal recessive spinocerebellar ataxia 23 DOID_0111613 [An autosomal recessive cerebellar ataxia characterized by epilepsy, intellectual disability, and gait ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the TDP2 gene on chromosome 6p22.3.]
ovarian endometrioid cystadenoma DOID_7191 [An ovarian cystadenoma that is characterized by the presence of endometrial tissue.]
autosomal recessive spinocerebellar ataxia 22 DOID_0111614 [An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the VWA3B gene on chromosome 2q11.2.]
Sporothrix schenckii NCBITaxon_29908
Sporothrix NCBITaxon_29907
autosomal recessive spinocerebellar ataxia 4 DOID_0111611 [An autosomal recessive cerebellar ataxia characterized by ataxic gait with spasticity, hyperreflexia of the lower limbs, and mitochondrial defects that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13D gene on chromosome 1p36.22-p36.21.]
obsolete autosomal recessive spinocerebellar ataxia 3 DOID_0111612 [An autosomal recessive cerebellar ataxia characterized by spinocerebellar ataxia with optic and cochlear degeneration that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 6p23-p21.]
distal arthrogryposis type 4 DOID_0111610 [A distal arthrogryposis characterized by distal arthrogryposis with severe scoliosis.]
distal arthrogryposis DOID_0050646 [A muscle tissue disease characterized by congenital joint contractures of hand and feet.]
hereditary conventional renal cell carcinoma DOID_7192
subacute lymphocytic thyroiditis DOID_7187
thyroiditis DOID_7166