All terms in DOID

Label Id Description
visceral pain SYMP_0000833 [A pain that is characterized by originating from organ tissues of the thorax, abdomen, or pelvis. It characterizes as deep, vague, and difficult to locate pain, that radiates away from the affected organ.]
nephrotic syndrome type 10 DOID_0080386 [A familial nephrotic syndrome characterized by early childhood onset that has_material_basis_in homozygous or compound heterozygous mutation in the EMP2 gene on chromosome 16p13.]
hypoesthesia SYMP_0000834 [A sensation perception that is characterized by a reduced sense of touch or sensation, or a partial loss of sensitivity to sensory stimuli.]
nephrotic syndrome type 12 DOID_0080387 [A familial nephrotic syndrome characterized by early childhood onset of steroid-resistant progressive renal failure with focal segmental glomerulosclerosis that has_material_basis_in homozygous or compound heterozygous mutation in the NUP93 gene on chromosome 16q13.]
nociceptive pain SYMP_0000831 [A pain that is characterized by originating from other than the peripheral and central nervous systems, and which is caused by activation of nociceptive fibers.]
nephrotic syndrome type 7 DOID_0080388 [A familial nephrotic syndrome characterized by onset in the first decade of life of progressive renal disease with proteinuria and membranoproliferative glomerulonephritis that has_material_basis_in homozygous or compound heterozygous mutation in the DGKE gene on chromosome 17q22.]
neuropathic pain SYMP_0000832 [A pain that is characterized by being experienced by cancer patients and which is caused by radiotherapy or chemotherapy damage to nerves, when cancer invades or compresses nerves, or when, during cancer treatment. This type of pain is typically described as burning, electrical, or strange feeling.]
nephrotic syndrome type 8 DOID_0080389 [A familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25.]
obsolete diabetes mellitus juvenile type, uncontrolled, with neurological manifestations DOID_10469
chronic laryngitis DOID_11797 [A laryngitis in which symptoms last longer than three weeks. Gastroesophageal reflux, and lingering bronchitis can cause the disease.]
obsolete ovarian dermoid cyst with secondary melanocytic lesion DOID_7590
gestational ovarian choriocarcinoma DOID_7591 [A choriocarcinoma of the ovary that develops in the presence of a preceding gestational event.]
acute pain SYMP_0000839 [A pain that is characterized by being severe but lasting a relatively short time.]
phthisical cornea DOID_11793
glottis verrucous carcinoma DOID_7583
glottis squamous cell carcinoma DOID_7031 [A squamous cell carcinoma that is located_in the glottis.]
subglottis verrucous carcinoma DOID_7584
subglottis squamous cell carcinoma DOID_7585
obsolete psychogenic depressive psychosis DOID_7581
obsolete Epstein-Barr virus related carcinoma DOID_6250 [An Epstein-Barr virus infectious disease and is_a carcinoma that derives_from epithelial cells, has_material_basis_in Human herpesvirus 4, which causes a growth activation of the epithelial cells that it infects.]