All terms in DOID

Label Id Description
obsolete Hodgkin's lymphoma, nodular sclerosis, involving lymph nodes of inguinal region and lower limb DOID_8978
anaphylactic shock SYMP_0000895 [An acute allergic reaction to an antigen to which the body has become hypersensitive.]
obsolete malignant histiocytosis involving lymph nodes of head, face, and neck DOID_8977
Bartholin's gland adenocarcinoma DOID_6316 [A Bartholin's gland carcinoma that derives_from epithelial cells originating in glandular tissue.]
exophthalmos SYMP_0000896 [An abnormal protrusion or displacement of an eye or other body part.]
obsolete peripheral lymph node tuberculosis DOID_8976
clivus chondroid chordoma DOID_6313 [A chondroid chordoma and chordoma of the clivus that is located_in the clivus.]
hypotensive SYMP_0000893 [A low blood pressure characterized by or due to abnormally low blood pressure, especially in the arteries of the systemic circulation.]
low blood pressure SYMP_0000692
ovarian fetiform teratoma DOID_6314 [A mature teratoma of the ovary that resembles a malformed human fetus with the caudal portion being more developed.]
cold clammy skin SYMP_0000894 [A skin and integumentary tissue symptom that is characterized by cold, moist and sticky skin.]
obsolete Hodgkin's lymphoma, lymphocytic depletion, involving intrapelvic lymph nodes DOID_8979
relapsing fever SYMP_0000890 [A fever that is characterized by body temperature periodically rising and falling.]
obsolete malignant skin blue nevus DOID_10053
expressive language disorder DOID_11385 [A language disorder that involves difficulties with verbal and written expression characterized by an ability to use expressive spoken language that is markedly below the appropriate level for the mental age, but with a language comprehension that is within normal limits.]
familial focal epilepsy with variable foci 4 DOID_0081424 [A familial focal epilepsy with variable foci that is characterized by onset of focal seizures in the first years of life and that has_material_basis_in heterozygous mutation in the SCN3A gene on chromosome 2q24.]
familial focal epilepsy with variable foci DOID_0081420 [A focal epilepsy that is characterized by focal seizures, with seizure onset in a discrete area of the brain including the temporal, frontal, parietal, and occipital lobes, with focal seizures arising from different cortical regions in different family members.]
skin amelanotic melanoma DOID_10054 [A skin melanoma that is characterized by a lack of melanin pigment in most of the melanoma tumor cells.]
autosomal recessive distal hereditary motor neuronopathy 6 DOID_0081425 [An autosomal recessive distal hereditary motor neuronopathy characterized by onset of distal muscle weakness in early infancy and that has_material_basis_in homozygous mutation in the REEP1 gene on chromosome 2p11.]
autosomal recessive distal hereditary motor neuronopathy DOID_0111197 [A spinal muscular atrophy that has_material_basis_in autosomal recessive inheritance.]