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Gaucher-like disease

Also Known As:

Pseudo Gaucher disease

Networked: 2 relevant articles (0 outcomes, 0 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
        Gaucher-like 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

Experts

1.	Al-Jasmi, Amina: 1 article (06/2022)
2.	Al-Jasmi, Fatma: 1 article (06/2022)
3.	Al-Tenaiji, Amal: 1 article (06/2022)
4.	Ali, Amanat: 1 article (06/2022)
5.	Mohamed, Feda E: 1 article (06/2022)
6.	Matsuda, Junko: 1 article (08/2010)
7.	Suzuki, Kinuko: 1 article (08/2010)
8.	Suzuki, Kunihiko: 1 article (08/2010)
9.	Yoneshige, Azusa: 1 article (08/2010)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Gaucher-like disease:

1.	SaposinsIBA 06/01/2022 - "A Type 3 Gaucher-Like Disease Due To Saposin C Deficiency in Two Emirati Families Caused by a Novel Splice Site Variant in the PSAP Gene." 08/01/2010 - "Humans with saposin C deficiency exhibit the clinical presentation of Gaucher-like disease. "