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Silver-Russell syndrome
rareSilver-Russell syndrome is characterized by growth retardation with antenatal onset, characteristic facies and limb asymmetry.
- Identifiers
- MONDO:0008394 Orphanet:813
- Part of
- Chromosomal disorderHereditary diseaseMultiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndromeSyndromic disease
- Also known as
- Russell Silver syndrome · Russell-Silver dwarfism · Russell-Silver Syndrome · Silver Russell syndrome · Silver-Russell dwarfism
Subtypes
Disease
- Russell-silver syndrome, X-linked MONDO:0010727
- Silver-Russell syndrome 1 MONDO:0020796
- Silver-Russell syndrome 3 MONDO:0014663 IGF2
- Silver-Russell syndrome 5 MONDO:0020795 HMGA2
- Silver-Russell syndrome due to 11p15 microduplication MONDO:0016481
- Silver-Russell syndrome due to 7p11.2p13 microduplication MONDO:0016479
- Silver-Russell syndrome due to an imprinting defect of 11p15 MONDO:0016480
- Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11 MONDO:0016482
- Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7 MONDO:0019913
- Silver-russell syndrome 2 MONDO:0030116
- Silver-russell syndrome 4 MONDO:0030118 PLAG1
Projects
Including projects on subtypes.
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