All terms in DOID
| Label | Id | Description |
|---|---|---|
| obsolete catatonic schizophrenia in remission | DOID_12204 | |
| purulent labyrinthitis | DOID_13534 | [A labyrinthitis which is a bacterial infectious disease of the inner ear, often causing deafness and loss of vestibular function. This is caused when bacteria spread to the inner ear during the course of severe acute otitis media, purulent meningitis, or an enlarging cholesteatoma.] |
| labyrinthitis | DOID_1468 | [An otitis interna which involves inflammation of the labyrinths.] |
| osteopetrosis | DOID_13533 | [An osteosclerosis that has_material_basis_in lack of bone resorption which results_in abnormally hard and brittle bones.] |
| granulocyte | CL_0000094 | |
| myeloid leukocyte | CL_0000766 | |
| obsolete Wuchereria bancrofti filariasis | DOID_12210 | [A filarial elephantiasis that involves parasitic infection of the lymphatic system by a filarial worm Wuchereria bancrofti, which is transmitted by mosquitoes. The symptoms include lymphedema, fever, chills, skin infections, painful lymph nodes, orchitis and epididymitis.] |
| interval angle-closure glaucoma | DOID_13549 | |
| secondary Parkinson disease | DOID_13548 | |
| Lewy body dementia | DOID_12217 | [A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities.] |
| oligohydramnios | DOID_12215 | [A placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion.] |
| hyperparathyroidism | DOID_13543 | [A parathyroid gland disease characterized by an overactivity of the parathyroid glands, leading to an excess of parathyroid hormone in the body.] |
| parathyroid gland disease | DOID_11201 | [An endocrine system disease that is located_in the parathyroid gland.] |
| filarial elephantiasis | DOID_12211 | [A filariasis that is characterized by the thickening of the skin and underlying tissues, especially in the legs, male genitals and female breasts, caused by thread-like parasitic worms Wuchereria bancrofti, Brugia malayi or Brugia timori, which inhabit the lymphatics. These nematodes are transmitted by mosquitoes. Acute symptoms include fever, lymphadenitis, lymphangitis, funiculitis, and epididymitis. Chronic symptoms include abscesses, hyperkeratosis, polyarthritis, hydroceles, lymphedema, and elephantiasis.] |
| bejel | DOID_13431 | [A primary bacterial infectious disease that results in infection located in mucosa of mouth, located in skin or located in bone, has_material_basis_in Treponema pallidum subsp endemicum, which is transmitted by contact or transmitted by sharing of domestic utensils. The infection has symptom moist patches in the mouth, has symptom lumps in long bones, tissues around the mouth, nose, and roof of the mouth. These lumps destroy tissue, causing bones to be deformed and disfiguring the face.] |
| postural orthostatic tachycardia syndrome | DOID_0111154 | [A heart conduction disease characterized by orthostatic intolerance that has_material_basis_in heterozygous mutation in the SLC6A2 gene on chromosome 16q12.2.] |
| Larsen syndrome | DOID_14764 | [Asyndrome that is characterized by autosomal dominant inheritance of large-joint dislocations and characteristic craniofacial abnormalities.] |
| autosomal recessive spinocerebellar ataxia 21 | DOID_0111155 | [An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.] |
| multicentric Castleman disease | DOID_0111152 | [A Castleman disease characterized by systemic inflammatory symptoms, polyclonal lymphoproliferation, cytopenias, and multiple organ system dysfunction caused by a cytokine storm often including interleukin-6.] |
| Castleman disease | DOID_0111157 | [A lymphoproliferative syndrome characterized by one or more enlarged lymph nodes containing cells with hyaline-vascular, plasmacytic, or mixed appearance microscopically.] |