All terms in MeSH

Label Id Description
Teratozoospermia D000072660 [Conditions in which sperm show abnormal morphology. ]
ganluotong C000600391
Ciliopathies D000072661 [Genetic disorders caused by defects in genes related to the primary CILIUM; BASAL BODY; or CENTROSOME. Primary features may include obesity, SKELETAL DYSPLASIA; POLYDACTYLY and malformations that primarily involve the liver, eye or kidneys. ]
Margins of Excision D000072662 [The edges of tissue removed in a surgery for assessment of the effectiveness of a surgical procedure in achieving the local control of a neoplasm and the adequacy of tumor removal. When the margin is negative or not involved by tumor (e.g., CANCER) it suggests all of the tumor has been removed by the surgery. ]
Spontaneous Perforation D000072663 [A pathological hole in an organ, blood vessel or other soft part of the body, occurring in the absence of external force. ]
Provitamins D000072664 [Precursor forms of vitamins. ]
National Center for Advancing Translational Sciences (U.S.) D000072666 [A unit of the National Institutes of Health that seeks to catalyze the generation of innovative methods and technologies that will enhance the development, testing, and implementation of diagnostics and therapeutics across a wide range of human diseases and conditions. The Center was established in 2011. ]
B9309-068 C114000
IMC-76 C000589551
National Center for Complementary and Integrative Health (U.S.) D000072667 [The mission of NCCIH is to define, through rigorous scientific investigation, the usefulness and safety of complementary and integrative health interventions and their roles in improving health and health care. The Center was established in 1999 and was known as NCCAM National Center of Complementary and Alternative Medicine until 2015. ]
Congenital idiopathic intestinal pseudoobstruction C535532
IMC-48 C000589552
Splicing Factor U2AF D000072668 [An RNA splicing factor that performs a critical function in both constitutive and enhancer-dependent RNA SPLICING. It recruits RIBONUCLEOPROTEIN, U2 SMALL NUCLEAR to the splice site and mediates interactions between it, the RNA molecule, and other splicing factors for accurate 3'-splice site selection. ]
graminin B C000589553
Gene Editing D000072669 [Genetic engineering or molecular biology techniques that involve DNA REPAIR mechanisms for incorporating site-specific modifications into a cell's genome. ]
Iridogoniodysgenesis and skeletal anomalies C535534
TMP920 C000589554
Iridogoniodysgenesis type1 C535535
Iridogoniodysgenesis, dominant type C535536
Iris dysplasia hypertelorism deafness C535537