All terms in MeSH

Label Id Description
Trichorrhexis nodosa syndrome C536556
Trichoscyphodysplasia C536557
Trichostasis spinulosa C536558
Nitrergic Neurons D026602 [Nerve cells where transmission is mediated by NITRIC OXIDE. ]
D-Aspartic Acid D026603 [The D-isomer of ASPARTIC ACID. ]
Craniometaphyseal dysplasia, autosomal recessive type C536570
Boerhaave syndrome C536571
Bone Marrow failure syndromes C536572
Boomerang dysplasia C536573
Bor-Duane hydrocephalus contiguous gene syndrome C536574
Borjeson-Forssman-Lehmann syndrome C536575
Bork Stender Schmidt syndrome C536576
Protein D-Aspartate-L-Isoaspartate Methyltransferase D026601 [A PROTEIN O-METHYLTRANSFERASE that recognizes and catalyzes the methyl esterification of ISOASPARTIC ACID and D-ASPARTIC ACID residues in peptides and proteins. It initiates the repair of proteins damaged by the spontaneous decomposition of normal L-aspartic acid and L-asparagine residues. ]
Walbaum Titran Durieux Crepin syndrome C536566
Waldmann disease C536567
Walker Dyson syndrome C536568
P26OLF protein, Rana catesbeiana C115659
BM 212 C115651
multiadhesive protein, Geodia cydonium C115652
N,N'-di(3-pyrrol-1-ylpropyl)-4,4'-bipyridine C115653