All terms in DOID

Label Id Description
systemic vein UBERON_0013140
flushing SYMP_0000511 [A skin and integumentary tissue symptom that is characterized by a markedly red flush in a persons face and often other areas of the skin, from various physiological conditions. Flushing is generally distinguished, despite a close physiological relation between them, from blushing, which is milder, generally restricted to the face or cheeks, and generally assumed to reflect embarrassment. Flushing is also a cardinal symptom of carcinoid syndrome the syndrome that results from hormones (often serotonin or histamine) being secreted into systemic circulation.]
paraurethral gland UBERON_0010145
female reproductive gland UBERON_0005398
male accessory sex gland UBERON_0010147
male reproductive gland UBERON_0005399
tachycardia SYMP_0000529 [Tachycardia is a cardiovascular system symptom consisting of a relatively rapid heart action whether physiological (as after exercise) or pathological.]
arrhythmia SYMP_0000287 [Arrhythmia is a cardiovascular system symptom consisting of an alteration in rhythm of the heartbeat either in time or force.]
undiagnosed cardiac murmur SYMP_0000527
transient alteration of awareness SYMP_0000525 [An alteration of consciousness that is characterized by a brief (transient) episode of losing normal awareness or behavior.]
ascites SYMP_0000526 [An abdominal symptom consisting of an abnormal accumulation of serous fluid in the spaces between tissues and organs in the cavity of the abdomen.]
anorexia SYMP_0000523 [A nutrition, metabolism, and development symptom that is characterized by a loss of appetite especially when prolonged.]
polyphagia SYMP_0000524 [A nutrition, metabolism, and development symptom that is characterized by an excessive appetite or eating.]
intestinal hypomagnesemia 1 DOID_0060883 [A hypomagnesemia characterized by very low serum magnesium levels due to defects in intestinal absorption and kidney excretion and secondary hypocalcemia that has_material_basis_in homozygous or compound heterozygous mutations in the TRPM6 gene on chromosome 9q21.]
renal hypomagnesemia 6 DOID_0060884 [A hypomagnesemia characterized by autosomal dominant inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has_material_basis_in heterozygous mutation in the CNNM2 gene on chromosome 10q24.]
renal hypomagnesemia 2 DOID_0060885 [A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has_material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23.]
osteopathia striata with cranial sclerosis DOID_0060886 [An osteosclerosis characterized by longitudinal striations of the metaphyses of the long bones, sclerosis of the craniofacial bones, macrocephaly, cleft palate and hearing loss in females and fetal or neonatal lethality in males that has_material_basis_in mutation in the AMER1 gene on chromosome Xq11.]
osteosclerosis DOID_4254 [A bone remodeling disease that results_in abnormal elevated bone density or mass.]
ossification of the posterior longitudinal ligament of spine DOID_0060887 [A connective tissue disease characterized by ectopic ossification of the posterior longitudinal spinal ligament resulting in spinal cord compression, myelopathy and hyperreflexia.]
transient myeloproliferative syndrome DOID_0060888 [A myeloproliferative neoplasm characterized by leukocytosis in newborns with Down syndrome.]