Cytoscape Web
Click node...

Fetal akinesia-cerebral and retinal hemorrhage syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
X-linked thrombocytopenia with normal platelets
1 OMIM reference -
1 associated gene
No signs/symptoms info
Fetal akinesia-cerebral and retinal hemorrhage syndrome
X-linked thrombocytopenia with normal platelets

DNM2
(UniProt - OMIM)
 WAS
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DNM2
(0.63)
WAS


Citations in the biomedical literature:


Fetal akinesia-cerebral and retinal hemorrhage syndrome
DNM2
X-linked thrombocytopenia with normal platelets
WAS



Fetal akinesia-cerebral and retinal hemorrhage syndrome
X-linked thrombocytopenia with normal platelets

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.