All terms in MeSH

Label Id Description
Lipase deficiency combined C535904
N(4)-hexadecyl-2'-deoxyribocytidylyl-(3',5')-3'-azido-2',3'-deoxythymidine C089811
Lipoatrophy with diabetes, hepatic steatosis, cardiomyopathy, and leukomelanodermic papules C535905
N(4)-palmitoyl-2'-deoxyribocytidylyl-(3',5')-3'-azido-2',3'-deoxythymidine C089812
Muscular dystrophy, limb-girdle, type 1A C535906
YO-PRO 1 C089813
prosomatostatin (29-92) C089814
Marcus Gunn phenomenon C535908
Marden Walker like syndrome C535909
Limb-girdle muscular dystrophy, type 2C C535900
Limb-girdle muscular dystrophy, type 2E C535902
acuB protein, Bacillus subtilis C089828
AcuC protein, Bacillus subtilis C089829
monosaccharide-hydrogen cotransporter C089820
Mononen Karnes Senac syndrome C535914
MS4A3 protein, human C089821
Cartilage hair hypoplasia like syndrome C535915
Ran-interacting protein p10, Xenopus C089822
Cartilage-hair hypoplasia C535916
bis(pivaloyloxymethyl)-9-(2-phosphonylmethoxyethyl)adenine C089823