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Intellectual deficit, X-linked, Snyder type
1 OMIM reference -
1 associated gene
10 connected diseases
No signs/symptoms info
Disease Type of connection
Encephalopathy due to hydroxykynureninuria
Alveolar soft-part sarcoma
Autosomal dominant spastic paraplegia type 13
Coffin-Lowry syndrome
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Translocation renal cell carcinoma
Weaver syndrome
X-linked non-syndromic intellectual deficit
Synonym(s):
- Snyder-Robinson syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SMS P52788300105
No signs/symptoms info available.