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1 OMIM reference -
14 associated genes
No signs/symptoms info
COMMON GENES: 1
3 associated genes
No signs/symptoms info
Microform holoprosencephaly
Situs inversus totalis

CDON CCDC11
DISP1 CITED2
DLL1 NODAL
FGF8
FOXH1
GAS1
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 inversus totalis
CCDC11 CITED2



Microform holoprosencephaly
Situs inversus totalis

Synonym(s):
- Microform HPE

Synonym(s):
- Complete situs inversus
- Complete situs inversus viscerum
- Situs inversus

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.