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 (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) |
|---|---|---|---|---|
| P15259 | PGAM2_HUMAN | glycogen storage disease 10 | p.Glu89Ala p.Arg90Trp p.Gly97Asp |
|