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Fetal akinesia-cerebral and retinal hemorrhage syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive centronuclear myopathy
1 OMIM reference -
2 associated genes
No signs/symptoms info
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Autosomal recessive centronuclear myopathy

DNM2
(UniProt - OMIM)
 BIN1
(UniProt - OMIM)
TTN
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DNM2
(0.52)
BIN1


Citations in the biomedical literature:


Fetal akinesia-cerebral and retinal hemorrhage syndrome
DNM2
Autosomal recessive centronuclear myopathy
BIN1 TTN



Fetal akinesia-cerebral and retinal hemorrhage syndrome
Autosomal recessive centronuclear myopathy

Synonym(s):
(no synonyms)

Synonym(s):
- AR-CNM
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
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:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.