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Overgrowth - macrocephaly - facial dysmorphism
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
17q11 microdeletion syndrome
Synonym(s):
- RNF135-related overgrowth syndrome
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
RNF135 Q8IUD6611358
No signs/symptoms info available.