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Type Iiic Gaucher Disease

Also Known As:

Gaucher Disease, Type Iiic

Networked: 2 relevant articles (0 outcomes, 1 trials/studies)

Disease Context: Research Results

Nervous System Diseases: 14178
- Central Nervous System Diseases: 4213
  - Brain Diseases: 15694
    - Metabolic Brain Diseases: 215
      - Inborn Metabolic Brain Diseases: 2
        Nervous System Lysosomal Storage Diseases
        Sphingolipidoses: 241
        Gaucher Disease: 3212
        Type Iiic Gaucher Disease: 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142

Related Diseases

1.	Pseudoxanthoma Elasticum (Gronblad Strandberg Syndrome)
2.	Progeria (Hutchinson Gilford Syndrome)
3.	Familial Hyperphosphatemic Tumoral Calcinosis
4.	Arterial calcification of infancy
5.	Singleton Merten syndrome

Experts

1.	Nitschke, Yvonne: 1 article (01/2017)
2.	Rutsch, Frank: 1 article (01/2017)
3.	Beutler, Ernest: 1 article (05/2007)
4.	Hungs, Marcel: 1 article (05/2007)
5.	Spear, Gerald S: 1 article (05/2007)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Type Iiic Gaucher Disease:

1.	DNA (Deoxyribonucleic Acid)IBA 05/01/2007 - "Studies of parental DNA were negative for the D409H mutation of type IIIc Gaucher disease. "
2.	Phosphates (Orthophosphate)IBA 01/01/2017 - "Based on the pathogenic principles causing the diseases, these can be classified into three groups: (1) disorders of an increased extracellular inorganic phosphate/inorganic pyrophosphate ratio (generalized arterial calcification of infancy, pseudoxanthoma elasticum, arterial calcification and distal joint calcification, progeria, idiopathic basal ganglia calcification, and hyperphosphatemic familial tumoral calcinosis; (2) interferonopathies (Singleton-Merten syndrome); and (3) others, including Keutel syndrome and Gaucher disease type IIIC. "
3.	diphosphoric acid (pyrophosphoric acid)IBA 01/01/2017 - "Based on the pathogenic principles causing the diseases, these can be classified into three groups: (1) disorders of an increased extracellular inorganic phosphate/inorganic pyrophosphate ratio (generalized arterial calcification of infancy, pseudoxanthoma elasticum, arterial calcification and distal joint calcification, progeria, idiopathic basal ganglia calcification, and hyperphosphatemic familial tumoral calcinosis; (2) interferonopathies (Singleton-Merten syndrome); and (3) others, including Keutel syndrome and Gaucher disease type IIIC. "