Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
intravascular angioleiomyoma	DOID_4266
angiomyoma	DOID_4265	[A leiomyoma that is located_in the blood vessels.]
fallopian tube papillary adenocarcinoma	DOID_5597	[A fallopian tube adenocarcinoma that is characterized by a papillary growth pattern.]
progressive pseudorheumatoid arthropathy of childhood	DOID_0090004	[A osteochondrodysplasia characterized by autosomal recessive inheritance with typical onset around 3 years of age, progressive severe degenerative joint disease, platyspondyly, epiphyseal enlargement but absence of inflammatory joint disease that has_material_basis_in homozygous or compound heterozygous mutation in the CHST3 gene on chromosome 10q22.]
pharyngitis	SYMP_0019150
Schwartz-Jampel syndrome 1	DOID_0090005	[A syndrome characterized by neuromyotonia and chondrodysplasia that has_material_basis_in hypomorphic mutations in the HSPG2 gene on chromosome 1p36.]
pulmonary edema	SYMP_0019151	[Pulmonary edema is a respiratory system and chest symptom characterized by an abnormal accumulation of fluid in the lungs.]
precursor T-lymphoblastic lymphoma/leukemia	DOID_5599
akinetic mutism	DOID_4267	[A brain disease characterized by marked reduction of nearly all motor functions including facial expressions, gestures and speech output, but with some degree of alertness.]
fallopian tube serous adenocarcinoma	DOID_5598	[A fallopian tube adenocarcinoma that derives_from epithelial cells originating in glandular tissue forming serous lesions.]
immunodeficiency-centromeric instability-facial anomalies syndrome 1	DOID_0090008	[An immunodeficiency-centromeric instability-facial anomalies syndrome characterized by autosomal recessive inheritance, facial dysmorphism and immunoglobulin deficiency of lymphocytes that has_material_basis_in homozygous or compound heterozygous mutation in the DNMT3B gene on chromosome 20q11.2.]
immunodeficiency-centromeric instability-facial anomalies syndrome 2	DOID_0090009	[An immunodeficiency-centromeric instability-facial anomalies syndrome characterized by autosomal recessive inheritance, facial dysmorphism, immunoglobulin deficiency resulting in recurrent infections, and mental retardation that has_material_basis_in homozygous or compound heterozygous mutation in the ZBTB24 gene on chromosome 6q21.]
susceptibility to familial breast-ovarian cancer 1	OMIM_604370
malaise	SYMP_0019176	[Malaise is a neurological and physiological symptom characterized as an indefinite feeling of debility or lack of health often indicative of or accompanying the onset of an illness.]
necrotic lesion	SYMP_0019178
lightheadedness	SYMP_0019179	[Lightheadedness is a neurological and physiological symptom characterized as the condition of being dizzy or on the verge of fainting, particularly when one arises to a standing position, is a predictable consequence of any medication tending to lower blood pressure.]
Mycoplasma pneumoniae	NCBITaxon_2104
Mycoplasma	NCBITaxon_2093
mediastinal mesenchymal tumor	DOID_5560
obsolete AIDS-related cervical Kaposi's sarcoma	DOID_6894