All terms in NCIT
| Label | Id | Description |
|---|---|---|
| STAT1 Gene | NCIT_C24831 | [This gene plays a role in signal transduction and activation of transcription. It is involved in cell organization/biogenesis.] |
| Exophytic | NCIT_C74938 | [Growing outward; developing externally.] |
| Adenosine Deaminase 2 Deficiency | NCIT_C126347 | [A disorder characterized by abnormal inflammation of various tissues, particularly the blood vessels, with intermittent. fevers, areas of net-like, mottled skin discoloration (livedo racemosa), hepatosplenomegaly, and recurrent strokes.] |
| Polyarteritis Nodosa | NCIT_C26847 | [A necrotizing vasculitis that affects medium-sized arteries, it is usually idiopathic, and may be triggered by viral infections (Hepatitis B, also others). A multisystem disease, it most commonly affects skin (nodules, livedo reticularis) and peripheral nerves; higher morbidity is associated with gastrointestinal, central nervous system, cardiac, and/or other organ involvement. Anti-neutrophil cytoplasmic antibodies (ANCA) are typically negative.] |
| Chronic Active EBV Infection of T-and NK-Cell Type, Systemic Form | NCIT_C126348 | [An on-going Epstein-Barr virus (EBV) infection characterized by repeated infectious mononucleosis-like symptoms, a very high titer of anti-EBV antibodies, and high levels of Epstein-Barr virus nucleic acids. Patients with CAEBV often develop progressive cellular and humoral immunodeficiency with pancytopenia and hypogammaglobulinemia.] |
| EBV Infection | NCIT_C38759 | [An infection that is caused by Epstein-Barr virus.] |
| GATA2 Deficiency | NCIT_C126349 | [A condition of decreased or absent presence or activity of endothelial transcription factor GATA-2 protein. Deficiency of this protein is associated with immunodeficiency 21 and autosomal dominant and sporadic monocytopenia and mycobacterial infection syndrome (MonoMAC).] |
| GATA2 Gene | NCIT_C97552 | [This gene is involved in both DNA binding and transcriptional regulation.] |
| Congenital Kyphosis | NCIT_C35325 | [An abnormally increased curvature of the thoracic portion of the spine that is present at the time of birth.] |
| Kyphosis | NCIT_C34754 | [Abnormally increased curvature of the thoracic portion of the spine.] |
| Congenital Lesion | NCIT_C53302 | |
| Deny | NCIT_C74933 | [Refuse to accept, recognize or acknowledge.] |
| STAT3 Deficiency | NCIT_C126342 | [A condition of decreased or absent presence or activity of signal transducer and activator of transcription 3 protein. Deficiency of this protein is associated with hyper-IgE syndrome.] |
| Hyperimmunoglobulin E Syndrome | NCIT_C3144 | [A condition that is characterized by elevated serum IgE, dermatitis, and respiratory infections.] |
| Chronic Periodontitis | NCIT_C35326 | [A chronic inflammatory process that affects the tissues that surround and support the teeth.] |
| Periodontitis | NCIT_C34918 | [An acute or chronic inflammatory process that affects the tissues that surround and support the teeth.] |
| Plasma Cell Labeling Index | NCIT_C74934 | [Any of various techniques for determining the s-phase fraction of bone marrow plasma cells. Traditionally, this test has been performed as a two color immunofluorescent microscope technique.] |
| DOCK8 Deficiency | NCIT_C126343 | [A condition of decreased or absent presence or activity of dedicator of cytokinesis protein 8. Deficiency of this protein is associated with autosomal recessive hyper-IgE recurrent infection syndrome.] |
| Broncho-Esophageal Fistula | NCIT_C35327 | [An abnormal connection between a bronchus and the esophagus.] |
| Fistula | NCIT_C3045 | [Abnormal epithelial-lined communication between two anatomical structures.] |