All terms in DOID

Label Id Description
histiocytosis DOID_3405 [A lymphatic system disease that is characterized by an excessive number of histiocytes.]
obsolete Henipavirus infectious disease DOID_4393 [A Paramyxoviridae infectious disease that results_in infection in domestic animals and humans, has_material_basis_in Henipavirus, which is transmitted_by direct contact with the urine, feces, and nasal secretions of an infected animal.]
abdominal segment skin UBERON_0003836
zone of skin UBERON_0000014
pustulosis of palm and sole DOID_4398
dicarboxylic aminoaciduria DOID_0060650 [An amino acid metabolic disorder that is characterized by an excess urinary excretion of aspartate and glutamate acidic amino acids.]
granulomatous dermatitis DOID_4397
obsolete taste disorder DOID_3067
MYH-9 related disease DOID_0060651 [A blood platelet disease that has_material_basis_in mutations in the MYH9 gene. It is characterized by thrombocytopenia, enlarged platelets, sensorineural hearing loss and presenile cataract.]
glioblastoma DOID_3068 [A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes.]
malignant astrocytoma DOID_3069 [A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord.]
acneiform dermatitis DOID_4399
cranial cavity UBERON_0013411
congenital hereditary endothelial dystrophy of cornea DOID_0060649 [A corneal endothelial dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the SLC4A11 gene, which encodes a sodium borate cotransporter, on chromosome 20p13 and is characterized by thickening and opacification of the cornea, altered morphology of the endothelium, and secretion of an abnormal collagenous layer at the Descemet membrane.]
susceptibility to familial meningioma MIM_607174
glycol ether CHEBI_172390 [A hydroxyether which contains both an ether and alcohol functional groups. It is one of the most versatile classes of organic solvents which are commonly used in paints, cleaners, adhesives, pharmaceuticals and cosmetics.]
endocrine-cerebro-osteodysplasia syndrome DOID_0060641 [A syndrome that is characterized by multiple congenital defects in endocrine, cerebral, and skeletal systems leading to neonatal mortality; it has_material_basis_in mutation in the gene encoding intestinal cell kinase.]
perfluoroalkyl substance CHEBI_172397 [An endocrine disruptor that is perfluoroalkyl substance, used widely in industrial applications, such as firefighting foams and non-stick pan, paper, and textile coatings.]
endochrine disruptor CHEBI_138015 [Any compound that can disrupt the functions of the endocrine (hormone) system.]
recessive dystrophic epidermolysis bullosa DOID_0060642 [An epidermolysis bullosa dystrophica characterized by recurrent blistering at the level of the sublamina densa beneath the cutaneous basement membrane; it has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding type VII collagen (COL7A1) on chromosome 3p21.]