Gaucher’s disease is caused by a mutation in the gene encoding glucocerebrosidase, leading to the accumulation of glucocerebroside in cells, particularly macrophages, and resulting in symptoms such as hepatomegaly and bone pain.
| List I | List II |
|---|---|
| A. Heart | III. Atrial natriuretic factor |
| B. Kidney | I. Erythropoietin |
| C. Gastrointestinal Tract | IV. Secretnin |
| D. Adrenal Cortex | II. Aldosterone |


