Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
histone_modification	SO_0001700	[Histone modification is a post translationally modified region whereby residues of the histone protein are modified by methylation, acetylation, phosphorylation, ubiquitination, sumoylation, citrullination, or ADP-ribosylation.]
H3K9_acetylation_site	SO_0001703	[A kind of histone modification site, whereby the 9th residue (a lysine), from the start of the H3 histone protein is acetylated.]
obsolete rickettsiosis	DOID_1709
H3K14_acetylation_site	SO_0001704	[A kind of histone modification site, whereby the 14th residue (a lysine), from the start of the H3 histone protein is acetylated.]
H3K4_monomethylation_site	SO_0001705	[A kind of histone modification, whereby the 4th residue (a lysine), from the start of the H3 protein is mono-methylated.]
H3K4_methylation_site	SO_0001734	[A kind of histone modification, whereby the 4th residue (a lysine), from the start of the H3 protein is methylated.]
H3K4_trimethylation	SO_0001706	[A kind of histone modification site, whereby the 4th residue (a lysine), from the start of the H3 protein is tri-methylated.]
Caroli disease	DOID_0050876	[A bile duct disease that is characterized by abnormal dilatation of the intrahepatic bile ducts.]
H3K9_trimethylation_site	SO_0001707	[A kind of histone modification site, whereby the 9th residue (a lysine), from the start of the H3 histone protein is tri-methylated.]
H3K9_methylation_site	SO_0001736	[A kind of histone modification site, whereby the 9th residue (a lysine), from the start of the H3 histone protein is methylated.]
obsolete small cell neuroendocrine carcinoma of the lung	DOID_0050875
H3K27_monomethylation_site	SO_0001708	[A kind of histone modification site, whereby the 27th residue (a lysine), from the start of the H3 histone protein is mono-methylated.]
H3K27_methylation_site	SO_0001732	[A kind of histone modification site, whereby the 27th residue (a lysine), from the start of the H3 histone protein is methylated.]
obsolete CLONE OF congenital afibrinogenemia	DOID_0050878
H3K27_trimethylation_site	SO_0001709	[A kind of histone modification site, whereby the 27th residue (a lysine), from the start of the H3 histone protein is tri-methylated.]
pancreatic agenesis	DOID_0050877	[A pancreas disease that is characterized by the failure of the pancreas to develop prior to birth.]
Richter's syndrome	DOID_1703
ichthyosis vulgaris	DOID_1702	[An ichthyosis that has_material_basis_in heterozygous mutation in the filaggrin gene on chromosome 1q21 and is characterized by dead skin cells accumulate in thick, dry scales on your skin's surface.]
fragile X-associated tremor/ataxia syndrome	DOID_0050879	[A X-linked hereditary ataxia that is characterized by adult-onset progressive intention tremor and gait ataxia, has_material_basis_in expanded trinucleotide repeat of the FMR1 gene that results_in a toxic gain of function of FMR1 RNA.]
colorectal adenocarcinoma	DOID_0050861	[A colorectal carcinoma that derives_from epithelial cells of glandular origin.]