Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
N6-Acetyl-L-lysine measurement	EFO_0021656	[Quantification of the amount of N6-Acetyl-L-lysine in a sample.]
Palmitaldehyde measurement	EFO_0021659	[Quantification of the amount of Palmitaldehyde in a sample.]
eugenol	CHEBI_4917	[A guaiacol with an allyl chain substituted para to the hydroxy group.]
Vocal cord paralysis	HP_0001605	[A loss of the ability to move the vocal folds.]
Vocal cord dysfunction	HP_0031801	[Any functional anomaly of the vocal cord.]
p-Hydroxyphenyl acetic acid measurement	EFO_0021658	[Quantification of the amount of p-Hydroxyphenyl acetic acid in a sample.]
N-acetyl-l-leucine measurement	EFO_0021653	[Quantification of the amount of N-acetyl-l-leucine in a sample.]
Myoinositol measurement	EFO_0021652	[Quantification of the amount of Myoinositol in a sample.]
Nasal speech	HP_0001611	[A type of speech characterized by the presence of an abnormally increased nasal airflow during speech.]
N,N-Dimethylglycine measurement	EFO_0021655	[Quantification of the amount of N,N-Dimethylglycine in a sample.]
N-Acetyl-L-tyrosine measurement	EFO_0021654	[Quantification of the amount of N-Acetyl-L-tyrosine in a sample.]
Methylmalonic acid measurement	EFO_0021651	[Quantification of the amount of Methylmalonic acid in a sample.]
Methionine sulfoxide measurement	EFO_0021650	[Quantification of the amount of Methionine sulfoxide in a sample.]
ChAP-seq	EFO_0008680	[Chromatin affinity precipitation (ChAP)-seq]
CHART	EFO_0008681	[Capture hybridization analysis of RNA targets (CHART)]
obsolete_glycogen storage disease due to lactate dehydrogenase H-subunit deficiency	Orphanet_284435
obsolete_Otopalatodigital syndrome	Orphanet_669	[Otopalatodigital (OPD) syndrome is a form of frontootopalatodigital syndrome (see this term), characterized by deafness, cleft palate, and characteristic digital anomalies. OPD syndrome is divided into two forms based on severity: the milder form designated OPD type 1 (OPD1), and the more severe and often lethal form designated OPD type 2 (OPD2; see these terms). OPD is an X-linked disorder. Two other genetic disorders with features overlapping OPD, frontometaphyseal dysplasia (FMD) and osteodysplasty, Melnick-Needles type (MNS) have been described; thus OPD1, OPD2, FMD, and MNS are allelic disorders.]
ChIPmentation	EFO_0008686	[Fast, robust, low-input ChIP-seq for histones and transcription factors]
obsolete_thyroid hemiagenesis	Orphanet_95719
ChIRP	EFO_0008687	[Chromatin Isolation by RNA Purification (ChIRP)]