Gaucher's disease
- Gaucher disease
Nature
A lipid storage disease linked to a single recessive gene particularly common in Jews of Eastern European ancestry. Gaucher disease results from a specific enzyme deficiency in the body, caused by a genetic mutation received from both parents. The disease course is quite variable, ranging from no outward symptoms to severe disability and death.
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Web link
SDG
Metadata
Database
World problems
Type
(E) Emanations of other problems
Biological classification
N/A
Subject
Medicine » Pathology
Content quality
Yet to rate
Language
English
1A4N
G5547
DOCID
11755470
D7NID
161132
Last update
Nov 3, 2022