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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Familial capillary hemangioma

DNM2 ANTXR1
KDR


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DNM2
(0.52)
KDR



Citations in the biomedical literature:


Fetal akinesia-cerebral and retinal hemorrhage syndrome
DNM2
Familial capillary hemangioma
ANTXR1 KDR



Fetal akinesia-cerebral and retinal hemorrhage syndrome
Familial capillary hemangioma

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -

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.