All terms in DOID

Label Id Description
temporal arteritis DOID_13375 [A central nervous system vasculitis that is characterized by inflammation of the lining of arteries, often arteries in the head.]
central nervous system vasculitis DOID_525 [A vasculitis that is characterized by inflammation of blood vessel walls in the brain or spine.]
fibrodysplasia ossificans progressiva DOID_13374 [A connective tissue disease that is characterized by progressive ossification of skeletal muscle, fascia, tendons, and ligaments and has_material_basis_in heterozygous mutation in the ACVR1 gene.]
kernicterus due to isoimmunization DOID_12043
Fanconi anemia complementation group J DOID_0111097 [A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BRIP1 gene on chromosome 17q22.]
Fanconi anemia complementation group B DOID_0111098 [A Fanconi anemia that has_material_basis_in mutation in the FANCB gene on chromosome Xp22.]
alpha 1-antitrypsin deficiency DOID_13372 [A plasma protein metabolism disease that has_material_basis_in defective production of the protease inhibitor alpha 1-antitrypsin (A1AT), leading to decreased A1AT activity in the blood and lungs, and deposition of excessive abnormal A1AT protein in liver cells.]
Fanconi anemia complementation group A DOID_0111095 [A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCA gene on chromosome 16q24.]
scrub typhus DOID_13371 [A typhus that has_material_basis_in Orientia tsutsugamushi, which is transmitted by trombiculid mites (Leptotrombidium deliense). The infection has symptom fever, has symptom headache, has symptom muscle pain, has symptom cough, has symptom maculopapular rash, has symptom eschar, has symptom splenomegaly and has symptom lymphadenopathy.]
typhus DOID_11256 [A primary bacterial infectious disease that refers to a group of diseases, located in endothelial cells of the small venous, arterial, and capillary vessels, has_material_basis_in Rickettsia bacteria, which are transmitted by lice, transmitted by fleas, and transmitted by mites.]
obsolete immune hydrops fetalis DOID_12040
Fanconi anemia complementation group O DOID_0111096 [A Fanconi anemia that has_material_basis_in homozygous mutation in the RAD51C gene on chromosome 17q21-q24.]
Fanconi anemia complementation group Q DOID_0111093 [A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the ERCC4 gene on chromosome 16p13.]
Fanconi anemia complementation group N DOID_0111094 [A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the PALB2 gene on chromosome 16p12.]
tetrachlorophthalic anhydride CHEBI_59097
Kawasaki disease DOID_13378 [A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels and that symptoms of fever, congestion of ocular conjunctivae, reddening of lips, reddening of oral cavity, protuberance of tongue papillae and edema of extremities.]
obsolete upper limb cancer DOID_13387
obsolete meningitis with clear cerebrospinal fluid DOID_12056
Fanconi anemia complementation group F DOID_0111088 [A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCF gene on chromosome 11p15.]
gastrointestinal anthrax DOID_13386 [An anthrax disease that results in infection located in mucosa of gastrointestinal tract, has_material_basis_in Bacillus anthracis, which is transmitted by ingestion of anthrax-infected meat. The infection has symptom lesions, has symptom vomiting of blood, has symptom severe diarrhea, has symptom loss of appetite.]