Browse MeSH Tree Structure
Diseases - (MeSH entry)
endocrine system diseases (0) +
congenital, hereditary, and neonatal diseases and abnormalities (1) +
disorders of environmental origin (0) +
bacterial infections and mycoses (0) +
substance-related disorders (0) +
musculoskeletal diseases (0) +
nutritional and metabolic diseases (1) +
digestive system diseases (0) +
male urogenital diseases (0) +
female urogenital diseases and pregnancy complications (0) +
otorhinolaryngologic diseases (0) +
pathological conditions, signs and symptoms (0) +
hemic and lymphatic diseases (1) +
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) |
|---|---|---|---|---|
| Q00597 | FANCC_HUMAN | p.Ser26Phe p.Ile80Thr p.Gly139Glu p.Leu190Phe p.Asp195Val p.Ile312Val p.Val449Met p.Gln465Arg p.Leu496Arg p.Leu554Pro |
| |
| Q00597 | FANCC_HUMAN | fanconi anemia complementation group c |