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14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
8 OMIM references -
8 associated genes
No signs/symptoms info
Semilobar holoprosencephaly
Atrial septal defect, ostium secundum type

CDON ACTC1
DISP1 CITED2
DLL1 GATA4
FGF8 GATA6
FOXH1 MYH6
GAS1 NKX2-5
GLI2 TBX20
NODAL TLL1
PTCH1
SHH
SIX3
TDGF1
TGIF1
ZIC2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FOXH1
(0.59)
NKX2-5



Citations in the biomedical literature:


Semilobar holoprosencephaly
CDON DISP1 DLL1 FGF8 FOXH1 GAS1
GLI2 NODAL PTCH1 SHH SIX3 TDGF1
TGIF1 ZIC2
Atrial septal defect, ostium secundum type
ACTC1 CITED2 GATA4 GATA6 MYH6 NKX2-5
TBX20 TLL1



Semilobar holoprosencephaly
Atrial septal defect, ostium secundum type

Synonym(s):
(no synonyms)

Synonym(s):
- ASD, ostium secundum type

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 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: -
Type of inheritance: multigenic/multifactorial
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
8 OMIM references -
No MeSH references

No signs/symptoms info available.