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Ceramidase deficiency (medical condition): A rare inherited biochemical disorder involving the deficiency of an enzyme called ceramidase resulting in the harmful accumulation of certain chemicals in the body which causes damage and inflammation.
See also:
Farber's disease:
»Introduction: Farber's disease
»Symptoms of Farber's disease
These medical condition or symptom topics may be relevant to medical information for Ceramidase deficiency:
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Ceramidase deficiency as a "rare disease".
Source - Orphanet
Ceramidase deficiency: Another name for Farber's disease (or close medical condition association).
»Introduction: Farber's disease
»Symptoms of Farber's disease
Some of the symptoms of Ceramidase deficiency incude:
See full list of 14 symptoms of Ceramidase deficiency (Farber's disease)
Source: Diseases Database
Source: Diseases Database
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