|
Worster Drought syndrome
|
C536747 |
|
|
Worth syndrome
|
C536748 |
|
|
Wright Dyck syndrome
|
C536749 |
|
|
BSM1 protein, Bos taurus
|
C115439 |
|
|
2-(4-(2-diethylaminoethoxy)phenylamino)-8-ethyl-6-phenyl-8H-pyrido(2,3-d)pyrimidin-7-one
|
C115431 |
|
|
FR 190809
|
C115432 |
|
|
FR 186485
|
C115433 |
|
|
E2f2 protein, Drosophila
|
C115434 |
|
|
JT95 monoclonal antibody
|
C115435 |
|
|
APLN protein, human
|
C115436 |
|
|
TRIM17 protein, human
|
C115437 |
|
|
contraception associated protein 1
|
C115438 |
|
|
Body Contouring
|
D000073880 |
[Plastic surgery to shape many areas of the body simultaneously. This may include LIPECTOMY or RHYTIDOPLASTY or both.
] |
|
Young Simpson syndrome
|
C536717 |
|
|
Young Syndrome
|
C536718 |
|
|
ATP Binding Cassette Transporter, Subfamily A, Member 4
|
D000073882 |
[An ATP binding cassette sub-family A transporter that translocates 11-cis and all-trans isomers of N-retinylidene-phosphatidylethanolamine (RETINOIDS) from the extracellular surface to the cytoplasmic membrane surface of RETINAL ROD CELLS and RETINAL CONE CELLS. Mutations in the ABCA4 gene are associated with Stargardt Disease 1, a hereditary juvenile form of MACULAR DEGENERATION.
] |
|
Yunis Varon syndrome
|
C536719 |
|
|
CX3C Chemokine Receptor 1
|
D000073883 |
[Receptor for CHEMOKINE CX3CL1 expressed by lymphocytes, neurons, and GLIAL CELLS. Its interaction with CX3CL1 mediates CELL ADHESION and CELL MIGRATION. It also functions as a co-receptor with the CD4 ANTIGEN for HIV-1 in vitro.
] |
|
C9orf72 Protein
|
D000073885 |
[A widely-expressed protein of approximately 400 to 500 amino acids. Its N-terminal region (DENN domain) interacts with RAB GTP-BINDING PROTEINS and may regulate AUTOPHAGY, as well as PROTEIN TRANSPORT to ENDOSOMES. Expansion of the GGGGCC hexanucleotide repeat in the first intron of the C9orf72 gene is associated with FRONTOTEMPORAL DEMENTIA with AMYOTROPHIC LATERAL SCLEROSIS (FTDALS1).
] |
|
BSM2 protein, Bos taurus
|
C115440 |
|
