Browse MeSH Tree Structure
Diseases - (MeSH entry)
endocrine system diseases (1) +
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 (1) +
female urogenital diseases and pregnancy complications (1) +
otorhinolaryngologic diseases (0) +
pathological conditions, signs and symptoms (0) +
hemic and lymphatic diseases (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) |
|---|---|---|---|---|
| P11168 | GTR2_HUMAN | p.Pro68Leu p.Val101Ile p.Thr110Ile p.Ile404Thr p.Leu478Val |
| |
| P11168 | GTR2_HUMAN | niddm | p.Val197Ile |
|
| P11168 | GTR2_HUMAN | fanconi-bickel syndrome | p.Leu389Pro p.Pro417Leu p.Val423Glu |
|