Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
pericarditis	DOID_1787	[A pericardium disease that is characterized by an inflammation of the pericardium and has_symptom chest pain.]
keratoconjunctivitis sicca	DOID_12895
dry eye syndrome	DOID_10140
blastema predominant kidney Wilms' tumor	DOID_5182
Sjogren's syndrome	DOID_12894	[An autoimmune hypersensitivity disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva.]
retinal vasculitis	DOID_11563	[A vasculitis that is characterized by inflammation of the vascular branches of the retinal artery and has_symptom painless decrease of visual acuity, visual floaters, dark spot in vision, decreased ability to distinguish colors, and distortion of images such as linear images.]
endometrium carcinoma in situ	DOID_5172	[An in situ carcinoma that is located_in the endometrium.]
renal Wilms' tumor	DOID_5176
mixed cell type kidney Wilms' tumor	DOID_5179
obsolete malignant neoplasm of pelvic bones, sacrum and coccyx	DOID_10239
metachronous kidney Wilms' tumor	DOID_5178
medium chain acyl-CoA dehydrogenase deficiency	DOID_0080153	[A lipid metabolism disorder that is characterized by a deficiency of the enzyme medium chain acyl-CoA dehydrogenase that results in the inability to convert medium chain fatty acids to energy, particularly during fasting.]
short chain acyl-CoA dehydrogenase deficiency	DOID_0080154	[A lipid metabolism disorder that is characterized by deficiency of the enzyme short chain acyl-CoA dehydrogenase that results in the inability to convert short chain fatty acids.]
adrenocorticotropic hormone deficiency	DOID_0080150	[A hypopituitarrium that is characterized by a decreased or absent production of adrenocorticotropic hormone by the pituitary gland.]
obsolete malignant neoplasm of pelvis	DOID_10240
Listeria meningitis	DOID_11572	[A bacterial meningitis that has_material_basis_in Listeria monocytogenes infection.]
mitochondrial DNA depletion syndrome 7	DOID_0080126	[A mitochondrial DNA depletion syndrome that is characterized by progressive ataxia, hypotonia, hyporeflexia, athetosis and sensory impairment and has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the C10ORF2 gene, which encodes the twinkle and twinky proteins, on chromosome 10q24.]
hemolytic anemia	DOID_583
mitochondrial DNA depletion syndrome 8a	DOID_0080127	[A mitochondrial DNA depletion syndrome that is characterized by neonatal hypotonia, lactic acidosis, and neurologic deterioration, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the ribonucleotide reductase regulatory TP53 inducible subunit M2B gene on chromosome 8q22.]
Abnormality of acid-base homeostasis	HP_0004360	[An abnormality of the balance or maintenance of the balance of acids and bases in bodily fluids, resulting in an abnormal pH.]