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Maternal uniparental disomy of chromosome 14
3 associated genes
No signs/symptoms info
COMMON GENES: 3
Paternal uniparental disomy of chromosome 14
1 OMIM reference -
3 associated genes
No signs/symptoms info
Maternal uniparental disomy of chromosome 14
Paternal uniparental disomy of chromosome 14

DLK1
(UniProt - OMIM)
 DLK1
(UniProt - OMIM)
MEG3
(UniProt - OMIM)
 MEG3
(UniProt - OMIM)
RTL1
(UniProt - OMIM)
 RTL1
(UniProt - OMIM)

COMMON
GENES 		DLK1
MEG3
RTL1


Citations in the biomedical literature:


Maternal uniparental disomy of chromosome 14
DLK1 MEG3 RTL1
Paternal uniparental disomy of chromosome 14



Maternal uniparental disomy of chromosome 14
Paternal uniparental disomy of chromosome 14

Synonym(s):
- UPD(14)mat
Synonym(s):
- UPD(14)pat
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C536471
No signs/symptoms info available.