|
obsolete depressive state induced by drug
|
DOID_11403 |
|
|
hypercementosis
|
DOID_12733 |
|
|
xanthogranulomatous pyelonephritis
|
DOID_11401 |
|
|
intermediate uveitis
|
DOID_12732 |
|
|
uveitis
|
DOID_13141 |
[An uveal disease is characterized by inflammation of any of the layers of the uvea of the eye, which includes the iris, ciliary body, and choroid.] |
|
pyelitis
|
DOID_2744 |
|
|
pars planitis
|
DOID_12731 |
|
|
chorioretinitis
|
DOID_8886 |
|
|
obsolete axillary cancer
|
DOID_5097 |
|
|
Omsk hemorrhagic fever virus
|
NCBITaxon_12542 |
|
|
Orthoflavivirus omskense
|
NCBITaxon_3048233 |
|
|
obsolete syphilitic disseminated chorioretinitis
|
DOID_11409 |
|
|
obsolete bronchial tuberculosis
|
DOID_12739 |
[A pulmonary tuberculosis which involves inflammation of bronchi resulting in irregular circumferential bronchial wall thickening that leads to narrowed or even obstructed airways.] |
|
gas molecular entity
|
CHEBI_138675 |
|
|
choroiditis
|
DOID_11406 |
|
|
choroid disease
|
DOID_1417 |
[An uveal disease that is located_in the choroid.] |
|
diphtheria
|
DOID_11405 |
[A primary bacterial infectious disease that is characterized by sore throat, low fever, and an adherent membrane (a pseudomembrane) on the tonsils, pharynx, and/or nasal cavity. A milder form of diphtheria can be restricted to the skin. It is caused by Corynebacterium diphtheriae, an aerobic Gram-positive bacterium. Diphtheria toxin spreads through the bloodstream and can lead to potentially life-threatening complications that affect other organs of the body, such as the heart and kidneys.] |
|
neural tube defect
|
DOID_0080074 |
[A physical disorder characterized by incomplete closure of the neural tube.] |
|
Neu-Laxova syndrome 2
|
DOID_0080075 |
[A serine deficiency that is characterized by multiple fatal malformations including ichthyosis, microcephaly, central nervous system abnormalities, limb deformities, intrauterine growth restriction, proptosis, anasarca, and micrognathia, and has_material_basis_in autosomal recessive inheritance of mutation in the PSAT1 gene on chromosome 9q21.1, causing issues producing the amino acid serine.] |
|
serine deficiency
|
DOID_0050721 |
[An amino acid metabolic disorder that has_material_basis_in defects in the biosynthesis of the amino acid L-serine.] |