All terms in DOID

Label Id Description
papilloma DOID_2615 [A cell type benign neoplam that is composed of epithelial tissue on papillae of vascularized connective tissue.]
Babesia NCBITaxon_5864
Babesiidae NCBITaxon_32594
skin papilloma DOID_3178 [A skin benign neoplasm that is composed of epithelial cells and a fibrous stalk.]
inverted papilloma DOID_3179
chromium atom CHEBI_28073
metal allergen CHEBI_88184
chromium group element atom CHEBI_33350
hypotonia-cystinuria syndrome DOID_0060858 [A syndrome that has_material_basis_in homozygous deletion on chromosome 2p21 that disrupts the SLC3A1 and PREPL genes. The deletion ranges in size from 23.8 to 75.5 kb. Itis characterized_by neonatal and infantile hypotonia and failure to thrive, cystinuria type 1 and nephrolithiasis, growth retardation due to growth hormone deficiency, and minor facial dysmorphism.]
salmonellosis DOID_0060859 [A primary bacterial infectious disease caused by the bacteria of the genus Salmonella. It has symptoms diarrhea, fever, vomiting, and abdominal cramps 12 to 72 hours after infection. In most cases, the illness lasts four to seven days, and most people recover without treatment.]
primary bacterial infectious disease DOID_0050338 [A bacterial infectious disease that results_in infection by bacteria as a result of their presence or activity within the normal, healthy host, and their intrinsic virulence is, in part, a necessary consequence of their need to reproduce and spread.]
Gastrointestinal dysmotility HP_0002579
Abnormal gastrointestinal motility HP_0030895
susceptibility to angioedema induced by ace inhibitors MIM_300909
annular pancreas DOID_0060850 [A pancreas disease characterized by autosomal dominant inheritance of the annular pancreas (head of the pancreas forming a ring around the second portion of the duodenum) and duodenal stenosis.]
pemphigus vulgaris DOID_0060851 [A pemphigus characterized by autosomal dominant blisters and erosions on the skin and mucous membranes erosions cause by autoantibodies to intercellular cement substance.]
pemphigus DOID_9182 [An autoimmune disease of skin and connective tissue that is characterized by blistering of the outer layer of the skin and mucous membranes (mouth, nose, throat, eyes, and genitals), causing lesions and blisters that are easily ruptured.]
Pierson syndrome DOID_0060852 [A syndrome characterized by nephrotic syndrome with diffuse mesangial sclerosis, proteinuria, microcoria, absence of the pupillary dilator muscle in the iris, ciliary muscle atrophy, and abnormal eye development with lens-shape, retinal and corneal anomalies that has_material_basis_in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p21.]
Potocki-Lupski syndrome DOID_0060853 [A chromosomal duplication syndrome characterized by hypotonia, failure to thrive, mental retardation, pervasive developmental disorders and congenital anomalies that has_material_basis_in contiguous gene syndrome caused by duplication of chromosome 17p11.2.]
autosomal recessive pseudohypoaldosteronism type 1 DOID_0060854 [A pseudohypoaldosteronism characterized by enal salt wasting and high concentrations of sodium in sweat, stool, and saliva that has_material_basis_in homozygous or compound heterozygous mutation in any one of 3 genes encoding subunits of the epithelial sodium channel (ENaC): SCNN1A, SCNN1B, or SCNN1G.]