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1 OMIM reference -
14 associated genes
No signs/symptoms info
COMMON GENES: 1
6 associated genes
No signs/symptoms info
Microform holoprosencephaly
Situs ambiguus

CDON ACVR2B
DISP1 CCDC11
DLL1 CFC1
FGF8 LEFTY2
FOXH1 NODAL
GAS1 ZIC3
GLI2
NODAL
PTCH1
SHH
SIX3
TDGF1
TGIF1
ZIC2


COMMON
GENES
NODAL



Citations in the biomedical literature:


Microform holoprosencephaly
CDON DISP1 DLL1 FGF8 FOXH1 GAS1
GLI2 NODAL PTCH1 SHH SIX3 TDGF1
TGIF1 ZIC2
Situs ambiguus
ACVR2B CCDC11 CFC1 LEFTY2 ZIC3



Microform holoprosencephaly
Situs ambiguus

Synonym(s):
- Microform HPE

Synonym(s):
- Incomplete situs inversus
- Partial situs inversus
- Situs ambiguous

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: adult
Type of inheritance: multigenic/multifactorial
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.