Terminology Service < Semantic Lookup Platform

All terms in MESH

Label	Id	Description
Chondrodysplasia Calcificans Metaphysealis	C565855
Cholestasis with Gallstone, Ataxia, and Visual Disturbance	C565856
ZNF256 protein, human	C526280
Sox7 protein, zebrafish	C526281
Periventricular Nodular Heterotopia	D054091	[A disorder resulting from a defect in the pattern of neuronal migration in which ectopic collections of neurons lie along the lateral ventricles of the brain or just beneath, contiguously or in isolated patches.]
Sox18 protein, zebrafish	C526282
Foramen Ovale, Patent	D054092	[A condition in which the FORAMEN OVALE in the ATRIAL SEPTUM fails to close shortly after birth. This results in abnormal communications between the two upper chambers of the heart. An isolated patent ovale foramen without other structural heart defects is usually of no hemodynamic significance.]
Heart Septal Defects, Atrial	D006344	[Developmental abnormalities in any portion of the ATRIAL SEPTUM resulting in abnormal communications between the two upper chambers of the heart. Classification of atrial septal defects is based on location of the communication and types of incomplete fusion of atrial septa with the ENDOCARDIAL CUSHIONS in the fetal heart. They include ostium primum, ostium secundum, sinus venosus, and coronary sinus defects.]
contactin 6 protein, mouse	C526283
polyoxyethylene 40 stearate	C526284
Car9 protein, rat	C526285
HLA-A*02:06 antigen	C526286
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism	C565850
ARC 1779	C526287
Chorea, Benign Familial	C565851
1,3-bis(benzylidene)-3,4-dihydro-1H-naphthalen-2-one	C526288
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome	C565852
2,6-bis(benzylidene)cyclohexanone	C526289
Chondrodysplasia Punctata Syndrome	C565853
3beta,6alpha,11,20beta,24-pentahydroxy- 9,11-seco-5alpha-24-ethylcholest-7,28-diene-9-one	C526247