Condition | Indicated | Relationship Strength | Studies | Trials |
Rida [description not available] | 0 | 3.61 | 9 | 0 |
Dementias, Transmissible [description not available] | 0 | 2.69 | 3 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 2.42 | 2 | 0 |
Nerve Degeneration Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways. | 0 | 2.04 | 1 | 0 |
Anasarca [description not available] | 0 | 2 | 1 | 0 |
Astrocytosis [description not available] | 0 | 2.41 | 2 | 0 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 2 | 1 | 0 |
HIV Human immunodeficiency virus. A non-taxonomic and historical term referring to any of two species, specifically HIV-1 and/or HIV-2. Prior to 1986, this was called human T-lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV). From 1986-1990, it was an official species called HIV. Since 1991, HIV was no longer considered an official species name; the two species were designated HIV-1 and HIV-2. | 0 | 2 | 1 | 0 |
Disease Exacerbation [description not available] | 0 | 2.91 | 1 | 0 |
CJD (Creutzfeldt-Jakob Disease) [description not available] | 0 | 2.91 | 1 | 0 |
Creutzfeldt-Jakob Syndrome A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27)) | 0 | 2.91 | 1 | 0 |
Aspergillus Infection [description not available] | 0 | 1.98 | 1 | 0 |
C gattii Infection [description not available] | 0 | 1.98 | 1 | 0 |
Fungal Diseases [description not available] | 0 | 1.98 | 1 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 1.98 | 1 | 0 |
Cryptococcosis Fungal infection caused by genus CRYPTOCOCCUS. | 0 | 1.98 | 1 | 0 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 1.98 | 1 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 1.98 | 1 | 0 |