Ceramidase deficiency

Introduction: Ceramidase deficiency

Description of Ceramidase deficiency

Ceramidase deficiency (medical condition): A rare inherited biochemical disorder involving the deficiency of an enzyme...more »

See also:

Farber's disease:
  »Introduction: Farber's disease
  »Symptoms of Farber's disease

Ceramidase deficiency: Related Topics

These medical condition or symptom topics may be relevant to medical information for Ceramidase deficiency:

• Ceramidase
• Deficiency
• Deficiency disease

Ceramidase deficiency: Rare Disease

Ophanet

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 as a Disease

Ceramidase deficiency: Another name for Farber's disease (or close medical condition association).
  »Introduction: Farber's disease
  »Symptoms of Farber's disease

Ceramidase deficiency: Related Diseases

Ceramidase deficiency: Ceramidase deficiency is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Metabolic conditions
• Congenital conditions - metabolic disorders
• Congenital conditions
• Lipid metabolism conditions

Symptoms of Ceramidase deficiency (Farber's disease)

Some of the symptoms of Ceramidase deficiency incude:

• Psychomotor deterioration
• Subcutaneous nodules
• Failure to thrive
• Swollen joints
• Mental retardation

See full list of 14 symptoms of Ceramidase deficiency (Farber's disease)

Terms associated with Ceramidase deficiency:

Terms Similar to Ceramidase deficiency:

• Disseminated lipogranulomatosis
• Farber's disease

Source: Diseases Database

External links related to: Ceramidase deficiency

• Farber's disease (www.whonamedit.com)
• OMIM - FARBER LIPOGRANULOMATOSIS

Source: Diseases Database

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

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