All terms in CLO
| Label | Id | Description |
|---|---|---|
| HEV0106 cell | CLO_0051261 | [Register: Imai, Takashi] |
| HEV0104 cell | CLO_0051260 | [Register: Imai, Takashi] |
| juvenile myoclonic epilepsy | DOID_4890 | |
| myoclonic epilepsy | DOID_308 | |
| hemophilia | DOID_2230 | |
| coagulation factor deficiency | DOID_2232 | |
| blood coagulation disorder | DOID_1247 | |
| simple genetic disease | DOID_0050177 | ["A hereditary disease that is the result of one or more abnormal alleles and may be dominant (a single copy of the abnormal allele is sufficient to give rise to the disease), semi-dominant, or recessive (requiring both copies of the gene to have an abnormal allele)." [DO:wk\,ls]] |
| partial epilepsy | DOID_2234 | |
| epilepsy | EFO_0000474 | [A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy) (MeSH)., A brain disorder characterized by episodes of abnormally increased neuronal discharge resulting in transient episodes of sensory or motor neurological dysfunction, or psychic dysfunction. These episodes may or may not be associated with loss of consciousness or convulsions.] |
| hypoprothrombinemia | DOID_2235 | |
| coagulation protein disorder | DOID_2212 | |
| hemorrhagic disorder | DOID_2213 | |
| inherited blood coagulation disorder | DOID_2214 | |
| adenocarcinoma in a polyp | DOID_4898 | |
| HEV0137 cell | CLO_0051269 | [Register: Imai, Takashi] |
| HEV0168 cell | CLO_0051279 | [Register: Imai, Takashi] |
| HEV0164 cell | CLO_0051278 | [Register: Imai, Takashi] |
| HEV0160 cell | CLO_0051277 | [Register: Imai, Takashi] |
| GM18945 cell | CLO_0026299 | [ INTERNATIONAL HAPMAP PROJECT - JAPANESE IN TOKYO, JAPAN INTERNATIONAL HAPMAP PROJECT - JAPANESE IN TOKYO AND HAN CHINESE IN BEIJING (PLATE I) CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19] |