Browse MeSH Tree Structure
Diseases - (MeSH entry)
hemic and lymphatic diseases (0) +
endocrine system diseases (0) +
chemically-induced disorders (0) +
otorhinolaryngologic diseases (0) +
digestive system diseases (0) +
musculoskeletal diseases (0) +
congenital, hereditary, and neonatal diseases and abnormalities (0) +
male urogenital diseases (0) +
respiratory tract diseases (0) +
bacterial infections and mycoses (0) +
skin and connective tissue diseases (0) +
female urogenital diseases and pregnancy complications (0) +
pathological conditions, signs and symptoms (0) +
Psychiatry and Psychology - (MeSH entry)
Disclaimer: The query results are intended for research purposes only, not for clinical and diagnostic use.
| Accession | Entry name | Disease | Variants | 3D mapping (variant position) |
|---|---|---|---|---|
| Q6PCD5 | RFWD3_HUMAN | fanconi anemia, complementation group w | p.Ile639Lys |
|