Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
purpuric rash	SYMP_0000660
recumbency	SYMP_0000661
obsolete actinic reticuloid and actinic granuloma	DOID_8749
obsolete acute dermatitis due to solar radiation	DOID_8748
mixed sleep apnea	DOID_0080302	[A sleep apnea that is characterized by a combination of central and obstructive sleep apnea.]
sleep apnea	DOID_0050847	[A sleep disorder characterized by repeated cessation and commencing of breathing that repeatedly disrupts sleep.]
mucinous lung adenocarcinoma	DOID_0080303	[A lung adenocarcinoma with tumor cells floating in pools of mucin that distend alveolar spaces.]
lung mucinous cystadenocarcinoma	DOID_0080304	[A lung adenocarcinoma that is a very rare malignant mucus-producing neoplasm arising from the uncontrolled growth of transformed epithelial cells originating in lung tissue.]
signet ring lung adenocarcinoma	DOID_0080305	[A lung adenocarcinoma containing a signet cell ring component characterized by abundant intracellular mucin accumulation and a displaced crescentic nucleus.]
acute dyspnea	SYMP_0000679
dyspnea	SYMP_0019153	[Dyspnea is a respiratory abnormality characterized by difficult or labored respiration.]
acute gastroenteritis	SYMP_0000677
acquired generalized lipodystrophy	DOID_0080300	[A complete generalized lipodystrophy that is charcterized by generalized disappearance of fat occurring during childhood and adolescence where normal body fat is present at birth.]
acute mental dysfunction	SYMP_0000678
atypical hemolytic-uremic syndrome	DOID_0080301	[A complement deficiency that is characterized by mechanical hemolytic anemia, thrombocytopenia, and renal dysfunction.]
complement deficiency	DOID_626	[A primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation.]
solid adenocarcinoma with mucin production	DOID_0080306	[A lung adenocarcinoma that lacks acini, tubules, and papillae, and contains many mucin-containing cells.]
myofibrillar myopathy 8	DOID_0080308	[A myofibrillar myopathy that is characterized by childhood onset of slowly progressive proximal muscle weakness and atrophy resulting in increased falls, gait problems, and difficulty running or climbing stairs, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the PYROXD1 gene on chromosome 12p12.]
fatal infantile hypertonic myofibrillar myopathy	DOID_0080309	[A myofibrillar myopathy that has_material_basis_in homozygous mutation in the CRYAB gene on chromosome 11q23.]
acute diarrhea	SYMP_0000675	[Acute diarrhea is a diarrhea with either or both a rapid onset or a short course.]