All terms in MeSH

Label Id Description
Piepkorn Karp Hickok syndrome C535774
Pierre Robin sequence with pectus excavatum and rib and scapular anomalies C535775
Pierre Robin syndrome with fetal chondrodysplasia C535776
Split hand foot deformity C535777
Spondylocamptodactyly C535779
6-(4-(3-(methylsulfonyl)benzylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)-3,4-dihydroquinolin-2(1H)-one C521108
dimethylsulfoxideimidazoletetrachlororuthenate(III) C075498
UGT89C1 protein, Arabidopsis C521109
2-N-carboxamidinonormianserin C075499
Congenital disorder of glycosylation type 1L C535750
Congenital disorder of glycosylation type 1X C535751
Gpr108 protein, mouse C521100
serum albumin, bovine (152-168) C075490
DNA polymerase delta p12 subunit, human C521101
isoxochitlolone C075492
Vwc2 protein, mouse C521103
xochitloldione C075493
2-methoxy-N-(3-(4-((3-methyl-4-((6-methyl-3-pyridinyl)oxy)phenyl)amino)-6-quinazolinyl)-2-propenyl)acetamide C521104
onopordopicrin C075494
dimethoxycurcumin C521105