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Silver-Russell syndrome due to 11p15 microduplication
2 associated genes
14 connected diseases
No signs/symptoms info
Disease Type of connection
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15
Hemihypertrophy
Silver-Russell syndrome due to imprinting defect of 11p15
Congenital atransferrinemia
Familial retinal arterial macroaneurysm
Congenital stromal corneal dystrophy
Growth delay due to insulin-like growth factor I resistance
Hyperinsulinism due to INSR deficiency
Hypoplasminogenemia
Insulin-resistance syndrome type A
Leprechaunism
Ligneous conjunctivitis
Rabson-Mendenhall syndrome
Simpson-Golabi-Behmel syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
H19 103280
IGF2 P01344147470
No signs/symptoms info available.