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14 associated genes
No signs/symptoms info
COMMON GENES: 14
PROTEIN INTERACTIONS: 4
14 associated genes
No signs/symptoms info
Semilobar holoprosencephaly
Lobar holoprosencephaly

CDON CDON
DISP1 DISP1
DLL1 DLL1
FGF8 FGF8
FOXH1 FOXH1
GAS1 GAS1
GLI2 GLI2
NODAL NODAL
PTCH1 PTCH1
SHH SHH
SIX3 SIX3
TDGF1 TDGF1
TGIF1 TGIF1
ZIC2 ZIC2


COMMON
GENES
CDON
DISP1
DLL1
FGF8
FOXH1
GAS1
GLI2
NODAL
PTCH1
SHH
SIX3
TDGF1
TGIF1
ZIC2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GLI2
FOXH1
PTCH1
GAS1
(0.73)
(0.72)
(0.59)
(0.55)
ZIC2
TGIF1
SHH
SHH



Citations in the biomedical literature:


Semilobar holoprosencephaly
CDON DISP1 DLL1 FGF8 FOXH1 GAS1
GLI2 NODAL PTCH1 SHH SIX3 TDGF1
TGIF1 ZIC2
Lobar holoprosencephaly





Semilobar holoprosencephaly
Lobar holoprosencephaly

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

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:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: multigenic/multifactorial

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.