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Silver-Russell syndrome due to an imprinting defect of 11p15

MedGen UID:: 1826102
•Concept ID:: C5680916
•: Disease or Syndrome

Synonym:	Chromosome 11p15.5-Related Russell-Silver Syndrome
Modes of inheritance:	Unknown inheritance MedGen UID: 989040 •Concept ID: CN307042 • Finding Source: Orphanet Hereditary clinical entity whose mode of inheritance is unknown. See: This record Not genetically inherited MedGen UID: 988794 •Concept ID: CN307044 • Finding Source: Orphanet clinical entity without genetic inheritance. See: This record Unknown inheritance (Orphanet) Not genetically inherited (Orphanet)

Monarch Initiative:	MONDO:0016480
Orphanet:	ORPHA231140

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVRussell-Silver syndrome
- CROGVSilver-Russell syndrome 1
  - CROGVSilver-Russell syndrome due to an imprinting defect of 11p15
- CROGVSilver-russell syndrome 2
- CROGVSilver-Russell syndrome 3
- CROGVSilver-russell syndrome 4
- CROGVSilver-Russell syndrome 5

Abnormality of prenatal development or birth
- Fetal anomaly
  - Congenital Systemic Disorder
    - Congenital anomaly of musculoskeletal system
      - Craniofacial Abnormalities
        Russell-Silver syndrome
        Silver-Russell syndrome due to an imprinting defect of 11p15

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