All terms in NCIT
| Label | Id | Description |
|---|---|---|
| Forty-Three | NCIT_C126587 | [A natural number greater than forty-two and less than forty-four and the quantity that it denotes.] |
| Pruritic Disorder | NCIT_C35101 | [A skin disorder characterized by an intense itching sensation.] |
| Transient Organic Mental Disorder | NCIT_C35102 | [An organic mental disorder that is temporary in nature.] |
| Organic Mental Disorder | NCIT_C34870 | [Any decrease in mental functioning in which the cause is not attributable to psychiatric illness, which includes damage from physical trauma, anoxic injury, damage from chemicals or toxins, infection, cancer, and degenerative diseases, including Alzheimer's disease, Huntington's disease, Parkinson's disease, and Creutzfeldt-Jakob disease.] |
| Uremia | NCIT_C35103 | |
| GP1BB wt Allele | NCIT_C126550 | [Human GP1BB wild-type allele is located in the vicinity of 22q11.21 and is approximately 2 kb in length. This allele, which encodes platelet glycoprotein Ib beta chain protein, plays a role in platelet aggregation. Mutation of the gene is associated with Bernard-Soulier syndrome type B.] |
| Nonpsychotic Mental Disorder Following Organic Brain Damage | NCIT_C35100 | [Any mental disorder that occurs secondary to organic brain damage, and that is not associated with psychosis.] |
| CCL3 wt Allele | NCIT_C49746 | [Human CCL3 wild-type allele is located within 17q11-q21 and is approximately 2 kb in length. This allele, which encodes C-C motif chemokine 3 protein, is involved in the acute inflammatory recruitment and activation of polymorphonuclear leukocytes.] |
| CCL3 Gene | NCIT_C24782 | [This gene is involved in intercellular communication.] |
| CCL3L1 wt Allele | NCIT_C49747 | [Human CCL3L1 wild-type allele in the vicinity of 17q21.1 and is approximately 2 kb in length. This allele, which encodes C-C motif chemokine 3-like 1 protein, is involved in leukocyte attraction and activation. CCL3L1 may play a role in both the cell cycle and signal transduction.] |
| CCL3L1 Gene | NCIT_C24783 | [This gene plays a role in immunoregulatory and inflammatory processes.] |
| CCL4 wt Allele | NCIT_C49748 | [Human CCL4 wild-type allele is located within 17q12 and is approximately 36 kb in length. This allele, which encodes C-C motif chemokine 4 protein, is involved in inflammatory processes.] |
| CCL4 Gene | NCIT_C24784 | [This gene plays a role in inflammatory and antiviral responses.] |
| CCL5 wt Allele | NCIT_C49749 | [Human CCL5 wild-type allele is located within 17q11.2-q12 and is approximately 36 kb in length. This allele, which encodes C-C motif chemokine 5 protein, plays a role in immune cell chemotaxis and histamine release.] |
| CCL5 Gene | NCIT_C24785 | [This gene plays a role in antiviral responses.] |
| CX3CL1 wt Allele | NCIT_C49753 | [Human CX3CL1 wild-type allele is located within 16q13 and is approximately 13 kb in length. This allele, which encodes fractalkine precursor protein, plays a role chemotaxis, signal transduction and cellular adhesion.] |
| CX3CL1 Gene | NCIT_C24796 | [This gene plays a role in both inflammatory processes and cellular adhesion.] |
| CXCL10 wt Allele | NCIT_C49756 | [Human CXCL10 wild-type allele is located within 4q21 and is approximately 2 kb in length. This allele, which encodes C-X-C motif chemokine 10 protein, plays a role in both immune cell migration and in the modulation of adhesion molecule expression.] |
| CXCL10 Gene | NCIT_C24788 | [This gene plays a role in immune system processes and is involved in angiogenesis.] |
| Hard Skin Syndrome Parana Type | NCIT_C126559 | [A rare disorder characterized by rigid, thick skin that covers the entire body and affects movements. The movement of the chest and abdomen is severely restricted. Affected individuals develop respiratory insufficiency which may lead to death.] |