All terms in DOID

Label Id Description
sulfur oxoacid derivative CHEBI_33424
tache noire SYMP_0000647 [A skin ulcer that is characterized by a a small dark-centered ulcer that appears at the site of a tick bite and is the primary lesion of boutonneuse fever.]
ruffled feather SYMP_0000644
Miura type epiphyseal chondrodysplasia DOID_0070316 [A bone developmental disease characterized by tall stature, scoliosis and macrodactyly of the great toes that has_material_basis_in heterozygous mutation in the NPR2 gene on chromosome 9p13.]
bone development disease DOID_0080006 [A bone disease that results_in abnormal growth and development located_in bone or located_in cartilage.]
wet beriberi DOID_0070317 [A beriberi that is located_in the cardiovascular system and has_symptom increased heart rate, swelling of lower legs, and shortness of breath.]
beriberi DOID_13725 [A thiamine deficiency disease that is characterized by being severe and chronic.]
obstructive nephropathy DOID_0070314 [A kidney disease characterized by kidney damage and dysfunction resulting from urinary tract obstruction.]
hypoplastic right heart syndrome DOID_0070315 [A congenital heart disease characterized by underdevelopment of the structures on the right side of the heart commonly associated with atrial septal defect.]
obsolete Peters-Plus Syndrome DOID_0070312 [A syndrome that is characterized by anterior chamber eye anomalies, short limbs with broad distal extremities, characteristic facial features, cleft lip or palate, and variable developmental delay or intellectual disability.]
nutritional deficiency disease DOID_5113 [A nutrition disease that is characterized by deficiency of a nutritional element, such as a vitamin, mineral, carbohydrate, protein, fat, or general energy content.]
drug-induced hearing loss DOID_0070310 [A nonsyndromic deafness that is characterized by cochlear or vestibular dysfunction resulting in loss of hearing caused by drug ototoxicity.]
nonsyndromic deafness DOID_0050563 [An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms.]
oligoasthenoteratozoospermia DOID_0070311 [A form of male infertility that is characterized by a combination of low number or oligozoospermia, poor motility or asthenozoospermia, and abnormal shape or teratozoospermia of sperms. OAT is the most common cause of male subfertility.]
male infertility DOID_12336
respiratory failure SYMP_0000643 [A respiratory system and chest symptom that is characterized by a difficulty to breathe on one's own and develops when the lungs cannot get enough oxygen into the blood.]
ankle rash SYMP_0000640 [A rash characterized by an inflammatory reaction of the skin on the ankles.]
renal involvement SYMP_0000641
Abnormal femur morphology HP_0002823
Abnormal lower limb bone morphology HP_0040069