Cytoscape Web
Click node...


1 OMIM reference -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 associated genes
No signs/symptoms info
Microform holoprosencephaly
Semantic dementia

CDON C9ORF72
DISP1 CHMP2B
DLL1 GRN
FGF8 MAPT
FOXH1 PSEN1
GAS1 VCP
GLI2
NODAL
PTCH1
SHH
SIX3
TDGF1
TGIF1
ZIC2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DLL1
(0.59)
PSEN1



Citations in the biomedical literature:


Microform holoprosencephaly
CDON DISP1 DLL1 FGF8 FOXH1 GAS1
GLI2 NODAL PTCH1 SHH SIX3 TDGF1
TGIF1 ZIC2
Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP



Microform holoprosencephaly
Semantic dementia

Synonym(s):
- Microform HPE

Synonym(s):
- Semantic primary progressive aphasia
- Semantic variant PPA

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -

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:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial

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

No signs/symptoms info available.