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2 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 2
1 OMIM reference -
14 associated genes
No signs/symptoms info
Radial hemimelia, bilateral
Microform holoprosencephaly

LMBR1 CDON
SHH DISP1
DLL1
FGF8
FOXH1
GAS1
GLI2
NODAL
PTCH1
SHH
SIX3
TDGF1
TGIF1
ZIC2


COMMON
GENES
SHH


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SHH
SHH
(0.59)
(0.55)
PTCH1
GAS1



Citations in the biomedical literature:


Radial hemimelia, bilateral
LMBR1 SHH
Microform holoprosencephaly
CDON DISP1 DLL1 FGF8 FOXH1 GAS1
GLI2 NODAL PTCH1 SIX3 TDGF1
TGIF1 ZIC2



Radial hemimelia, bilateral
Microform holoprosencephaly

Synonym(s):
- Radial longitidinal meromelia, bilateral

Synonym(s):
- Microform HPE

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

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

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

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

No signs/symptoms info available.