Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
Vascular Endothelial Growth Factor A 165 Isoform	NCIT_C126413	[Vascular endothelial growth factor A 165 isoform (191 aa, ~22 kDa) is encoded by the human VEGFA gene. This protein plays a role in the positive regulation of both cell proliferation and angiogenesis.]
APOBEC Family Protein	NCIT_C126414	[A family of enzymes involved in cytidine deamination, which converts cytidine into uracil, in DNA or RNA. These enzymes play a role in mRNA editing and retroviral host defenses.]
Cytidine Deaminase	NCIT_C48963	[Cytidine deaminase (146 aa, ~16 kDa) is encoded by the human CDA gene. This protein is involved in the deamination of cytidine and deoxycytidine to uridine and deoxyuridine, respectively.]
Line Cord Device Component	NCIT_C49891
HLA-KIR Compound Genotype	NCIT_C126415	[The combination of polymorphisms in the DNA encoding human leukocyte antigens (HLA) and killer-cell immunoglobulin-like receptors (KIR) found in an individual's genome. Certain combinations may indicate that the subject is more likely to develop certain diseases such as autoimmune disorders, viral infections, and cancer.]
Genotype	NCIT_C16631	[The genetic constitution of an organism or cell, as distinct from its expressed features or phenotype.]
Angiotensin II Measurement	NCIT_C74845	[The determination of the amount of angiotensin II hormone present in a sample.]
Angiotensinogen Measurement	NCIT_C74846	[The determination of the amount of angiotensinogen hormone present in a sample.]
Injury to Stomach with Open Wound into Cavity	NCIT_C35238	[Trauma to the stomach associated with a break in the tissue that extends into the abdominal cavity.]
Antidiuretic Hormone Measurement	NCIT_C74847	[The determination of the amount of antidiuretic hormone present in a sample.]
Injury to Duodenum with Open Wound into Cavity	NCIT_C35239	[Trauma to the duodenum associated with a break in the tissue that extends into the abdominal cavity.]
Thyroid Gland Papillary Carcinoma with Fibromatosis/Fasciitis-Like Stroma	NCIT_C126410	[A rare morphologic variant of papillary thyroid gland carcinoma characterized by the presence of abundant and cellular stroma resembling nodular fasciitis, fibromatosis, or other proliferative myofibroblastic processes. (WHO 2017)]
Calcitonin Measurement	NCIT_C74848	[The determination of the amount of calcitonin hormone present in a sample.]
Prominent Stromal Reaction	NCIT_C126411	[A morphologic finding indicating the presence of an exuberant proliferation of fibroblasts and myofibroblasts in the stroma of a tumor sample.]
Peripheral Nerve Infection with Unknown Absolute Neutrophil Count, CTCAE	NCIT_C60211
Greig Syndrome	NCIT_C35255	[An autosomal dominant genetic disorder caused by mutations in the GLI3 gene. It is characterized by physical abnormalities of the fingers and/or toes (extra fingers and/ or toes, fusion of the fingers and/or toes), large size head with prominent forehead and hypertelorism.]
Peristomal Infection Documented Clinically or Microbiologically with Grade 3 or 4 Neutrophils, CTCAE	NCIT_C60212
Aicardi Syndrome	NCIT_C35256	[A sporadic genetic syndrome characterized by agenesis of the corpus callosum, infantile spasms, and chorioretinal lacunae. It is associated with the presence of choroid plexus neoplasms in the brain.]
Choroid Plexus Papilloma	NCIT_C3698	[A benign, slow growing tumor which may cause symptoms by blocking cerebrospinal fluid pathways. It is characterized by the presence of delicate fibrovascular connective tissue fronds covered by a single layer of epithelial cells. Mitotic activity is extremely low. Surgical resection is usually curative. (Adapted from WHO)]
Peristomal Infection with Normal Absolute Neutrophil Count or Grade 1 or 2 Neutrophils, CTCAE	NCIT_C60213