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Sanfilippo syndrome type D
1 OMIM reference -
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
Chronic myeloid leukemia
Encephalopathy due to hydroxykynureninuria
Fabry disease
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Prolidase deficiency
Synonym(s):
- GNS deficiency
- Glucosamine N-acetyl-6-sulfatase deficiency
- Mucopolysaccharidosis type 3D
Classification (Orphanet):
- Inborn errors of metabolism
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
GNS P15586607664
No signs/symptoms info available.