All terms in NCIT
| Label | Id | Description |
|---|---|---|
| Gray Matter | NCIT_C32695 | [The nerve tissue composed of nerve cell bodies, unmyelinated nerve fibers and supportive tissue found in the brain and spinal cord. It is differentiated from the white matter by color of the tissues and the presence of more myelinated nerve cells in the white matter.] |
| Brain Part | NCIT_C13031 | [Any component of the central nervous system that is contained within the cranium.] |
| Frontal Pole | NCIT_C126737 | [The anterior pointed end of a cerebral hemisphere.] |
| Cerebral Hemisphere | NCIT_C12351 | [The part of the brain that controls muscle functions and also controls speech, thought, emotions, reading, writing, and learning. The right hemisphere controls the muscles on the left side of the body, and the left hemisphere controls the muscles on the right side of the body.] |
| Brain White Matter | NCIT_C49334 | |
| White Matter | NCIT_C33892 | [The nerve tissue forming the bulk of the deep parts of the brain and the superficial parts of the spinal cord. It is composed of nerve cell processes, i.e. extensions (axons), which connect various grey matter areas of the brain to each other and carry nerve impulses to and from the nerve cell bodies within the central nervous system (neurons). Cerebral and spinal white matter does not contain dendrites. White matter is distinguished in that it is composed of axonal nerve fibers covered by a myelin sheath.] |
| Phosphoglycerate Kinase 1 Deficiency | NCIT_C126738 | [An X-linked recessive inherited disorder caused by mutations in the PGK1 gene. Clinical manifestations include hemolytic anemia, myopathy, and neurologic involvement.] |
| Iodine I 123 RISAD-P | NCIT_C126731 | [A radioconjugate containing an androgen receptor (AR) targeting agent, 5-radioiodo-3'-O-(17beta-succinyl-5alpha-androstan-3-one)-2'-deoxyuridin-5'-yl phosphate (RISAD-P), labeled with the radioisotope iodine I 123 ([123]I-RISAD-P), with potential use as an imaging agent for single photon emission computed tomography (SPECT) imaging. Upon administration, iodine I 123 RISAD-P selectively binds to and is taken up by AR. Upon SPECT imaging, AR-expressing tumor cells can be imaged and AR expression levels can be assessed. AR, which is overexpressed on certain tumor cells, plays key roles in tumor cell growth and survival.] |
| Liver Progression GvHD | NCIT_C126732 | [An increase by two times the upper limit of normal for ALT, alkaline phosphatase, and total bilirubin.] |
| Lung Progression GvHD | NCIT_C126733 | [Either a decrease by 10% predicted absolute value of %FEV1 or an NIH lung symptom score that has increased by 1 or more points, except 0 to 1.] |
| Arterial System Smooth Muscle Tissue | NCIT_C49330 | [The smooth muscle tissue present in the tunica media which is the middle layer of the wall of the arterial system.] |
| Tunica Media | NCIT_C33821 | [The middle layer of the blood vessel wall. It consists of concentrically arranged smooth muscle and may include elastic tissue. Its thickness will depend on the type of vessel, thicker in arteries than in veins.] |
| Joints and Fascia Progression GvHD | NCIT_C126734 | [A NIH joint and fascia score that has increased by 1 or more points or a decrease in P-ROM score by 1 point for any site.] |
| Lower GI Progression GvHD | NCIT_C126730 | [An NIH lower GI score that has increased by 1 or more points, except 0 to 1.] |
| CD68 Gene | NCIT_C88921 | [This gene may be involved in macrophage homing, selectin recognition and pathogen uptake.] |
| Induced Mutation | NCIT_C40987 | [Any mutation that occurs in response to inducing agents, including radiation, viral infection, and a broad variety of mutagenic chemicals.] |
| Mutation Abnormality | NCIT_C45576 | [Any transmissible change in the genetic material of an organism, which can result from radiation, viral infection, transposition, treatment with mutagenic chemicals and errors during DNA replication or meiosis. The effects of mutation range from single base changes to loss or gain of complete chromosomes. As many of the simpler alterations to DNA may be repaired, such changes are only heritable once the change is fixed in the DNA by the process of replication. Mutations may be associated with genetic diversity or with pathologies including cancer.] |
| Case Report Form | NCIT_C40988 | [A printed, optical, or electronic document designed to record all of the clinical study-required information stipulated in the protocol to be reported to the sponsor on each clinical trial subject.] |
| Form | NCIT_C19464 | [A printed or electronic document with spaces to be filled out.] |
| CD68 wt Allele | NCIT_C88922 | [Human CD68 wild-type allele is located in the vicinity of 17p13 and is approximately 3 kb in length. This allele, which encodes macrosialin protein, may play a role in the regulation of macrophage homing and rolling and the mediation of pathogen binding and internalization.] |