Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
assortment_derived_deficiency_plus_duplication	SO_0000801	[A multi-chromosome aberration generated by reassortment of other aberration components; presumed to have a deficiency and a duplication.]
assortment_derived_duplication	SO_0000800	[A multi-chromosome duplication aberration generated by reassortment of other aberration components.]
susceptibility to dyslexia 1	OMIM_127700
atrioventricular septum	UBERON_0005989
cardiac septum	UBERON_0002099
food material	FOODON_00002403
Abnormality of amino acid metabolism	HP_0004337	[Abnormality of an amino acid metabolic process.]
mesentery	UBERON_0002095
Tangier disease	DOID_1388
hypolipoproteinemia	DOID_1387
abetalipoproteinemia	DOID_1386	[A hypolipoproteinemia that is characterized by an inablility to fully absorb dietary fats, cholesterol and fat-soluble vitamins, has_material_basis_in an autosomal recessive disorder of lipid metabolism that has_material_basis_in mutation in the microsomal triglyceride transfer protein that catalyzes the transport of lipids and is required in the secretion of BETA-LIPOPROTEINS.]
interventricular septum	UBERON_0002094
obsolete Chlamydia trachomatis urethritis	DOID_1384
Fox-Fordyce disease	DOID_1381	[A sweat gland disease that is characterized by dilatation of the follicular infundibulum with hyperkeratosis, acanthosis, and spongiosis with perifollicular inflammation leading to hair loss and has_symptom flesh colored papules with hair loss and pruritis, especially of the axilla.]
Dothideomycetes	NCBITaxon_147541
Pleosporomycetidae	NCBITaxon_451868
Eurotiomycetes	NCBITaxon_147545
primary lacrimal atrophy	DOID_1399
Abnormality of vitamin B metabolism	HP_0004340
Abnormality of vitamin metabolism	HP_0100508	[An anomaly in the metabolism of a vitamin.]