All terms in NCIT
| Label | Id | Description |
|---|---|---|
| Rat Cholangiofibrosis | NCIT_C60373 | |
| Rat Cholangioma | NCIT_C60374 | |
| Rat Chondroma | NCIT_C60375 | |
| Rat Cortical Adenoma | NCIT_C60380 | |
| Rat Cortical Carcinoma | NCIT_C60381 | |
| Rat Cortical Hyperplasia | NCIT_C60382 | |
| Rat Benign Hibernoma | NCIT_C60343 | |
| Rat Benign Luteoma | NCIT_C60344 | |
| Rat Benign Medullary Tumor | NCIT_C60345 | |
| Rat Benign Meningioma | NCIT_C60346 | |
| Rat Benign Granulosa Cell Tumor | NCIT_C60340 | |
| Rat Benign Hair Follicle Tumor | NCIT_C60341 | |
| Rat Benign Hemangiopericytoma | NCIT_C60342 | |
| Colony Forming Unit per Dish | NCIT_C74990 | [A derived unit of viable cell concentration defined as the number of colony forming units in one culture dish.] |
| Unit of Arbitrary Substance Concentration | NCIT_C67375 | [A unit of measurement of arbitrary quantity of substance (based on its biologic activity) in the unit volume of the system.] |
| Rat Benign Mesothelioma | NCIT_C60347 | |
| Rat Benign Mixed Glioma | NCIT_C60348 | |
| Rat Benign Mixed Muellerian Tumor | NCIT_C60349 | |
| Stickler Syndrome | NCIT_C74984 | [A rare autosomal dominant syndrome caused by mutations in the COL11A1, COL11A2, and COL2A1 genes which affect the production of type II and XI collagen. It is characterized by a range of signs and symptoms including cleft palate, large tongue, small lower jaw, hearing loss, myopia, glaucoma, retinal detachment, skeletal, and joint abnormalities.] |
| Stickler Syndrome Type 2 | NCIT_C74985 | [A rare autosomal dominant syndrome caused by mutations in the COL11A1 gene. It is characterized by an abnormal ocular vitreous architecture (beaded vitreous phenotype). Other signs and symptoms include retinal detachment, joint hypermobility, hearing loss, and midline clefting.] |