All terms in MeSH

Label Id Description
Triple X syndrome C535318
2,3,5-trihydroxy-5-(propylcarbamoyl)cyclohexyl 6-(4-ethoxy-6-methoxy-7-methyl-3-oxo-1,3-dihydroisobenzofuran-5-yl)-4-methylhex-4-enoate C000589734
49,XXXXX syndrome C535319
Chromosome 20, deletion 20p C535370
angustatin, Dendroaspis angusticeps C000600549
Trisomy 20p C535371
Chromosome 20, trisomy C535372
Dermatoosteolysis Kirghizian type C535373
Dermatopathia pigmentosa reticularis C535374
Dermochondrocorneal dystrophy of François C535375
Dermoids of cornea C535376
Epidermolysis bullosa with pyloric atresia C535377
Chromosome 2, trisomy 2q C535367
Chromosome 2, trisomy 2q37 C535368
Chromosome 20 ring C535369
Eryptosis D000072817 [Suicidal death of ERYTHROCYTES which results in features typical of apoptotic nucleated cells such as cell shrinkage, membrane blebbing, and scrambling of cell membrane to expose membrane PHOSPHATIDYLSERINES, which triggers engulfment and degradation by MACROPHAGES. ]
CPK32 protein, Arabidopsis C000589713
integracin A C574906
Arthrogryposis multiplex with deafness, inguinal hernias, and early death C535381
CNGC18 protein, Arabidopsis C000589714