All terms in NCIT
| Label | Id | Description |
|---|---|---|
| FACT-L Version 4 - I Have Been Coughing | NCIT_C151264 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Additional Concerns: I have been coughing.] |
| FACT-L Version 4 - Content With Quality of My Life | NCIT_C151260 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Functional Well-Being: I am content with the quality of my life right now.] |
| FACT-L Version 4 - Have You Ever Smoked | NCIT_C151269 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Additional Concerns: Have you ever smoked?] |
| FACT-L Version 4 - I Am Bothered by Hair Loss | NCIT_C151265 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Additional Concerns: I am bothered by hair loss.] |
| FACT-L Version 4 - I Have a Good Appetite | NCIT_C151266 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Additional Concerns: I have a good appetite.] |
| FACT-L Version 4 - I Feel Tightness in My Chest | NCIT_C151267 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Additional Concerns: I feel tightness in my chest.] |
| FACT-L Version 4 - Breathing Is Easy for Me | NCIT_C151268 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Additional Concerns: Breathing is easy for me.] |
| STXBP2 Deficiency | NCIT_C126294 | [A condition of decreased or absent presence of syntaxin-binding protein 2. Deficiency of this protein is associated with familial hemophagocytic lymphohistiocytosis type 5.] |
| Immunodeficiency Syndrome | NCIT_C3131 | [Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral.] |
| FACT-L Version 4 - Losing Hope Against Illness | NCIT_C151250 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Emotional Well-Being: I am losing hope in the fight against my illness.] |
| XIAP Deficiency | NCIT_C126295 | [A condition of decreased or absent presence of baculoviral IAP repeat-containing protein 4. Deficiency of this protein is associated with X-linked lymphoproliferative syndrome 2.] |
| FACT-L Version 4 - I Feel Nervous | NCIT_C151251 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Emotional Well-Being: I feel nervous.] |
| Immunodeficiency of Unknown Origin | NCIT_C126296 | [A condition of compromised immune function resulting from an uncharacterized defect.] |
| FACT-L Version 4 - I Worry About Dying | NCIT_C151252 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Emotional Well-Being: I worry about dying.] |
| Vector of Transplantation Incompatibility | NCIT_C126297 | [Refers to the direction of allorecognition between donor and recipient.] |
| FACT-L Version 4 - Worry My Condition Will Get Worse | NCIT_C151253 | [Functional Assessment of Cancer Therapy-Lung Version 4 (FACT-L Version 4) Emotional Well-Being: I worry that my condition will get worse.] |
| TERC Deficiency | NCIT_C126290 | [A condition of decreased or absent presence of telomerase RNA component. Deficiency of telomerase RNA component is associated with autosomal dominant dyskeratosis congenita 1, telomere-related pulmonary fibrosis, and bone marrow failure 2.] |
| TERT Deficiency | NCIT_C126291 | [A condition of decreased or absent presence of telomerase reverse transcriptase. Deficiency of this protein is associated with autosomal dominant dyskeratosis congenital 2, autosomal recessive dyskeratosis congenita 4, telomere-related pulmonary fibrosis, and bone marrow failure 1.] |
| Perforin Deficiency | NCIT_C126292 | [A condition of decreased or absent presence of perforin. Deficiency of this protein is associated with T-cell lymphoblastic lymphoma, aplastic anemia, hemophagocytic lymphohistiocytosis familial type 2, autoimmune lymphoproliferative syndrome and other lymphoproliferative disorders, including various forms of lymphoma.] |
| UNC13D Deficiency | NCIT_C126293 | [A condition of decreased or absent presence of protein unc-13 homolog D. Deficiency of this protein is associated with familial hemophagocytic lymphohistiocytosis 3.] |