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Fetal akinesia-cerebral and retinal hemorrhage syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal dominant Charcot-Marie-Tooth disease type 2M
1 OMIM reference -
1 associated gene
No signs/symptoms info
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2M

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

COMMON
GENES 		DNM2


Citations in the biomedical literature:


Fetal akinesia-cerebral and retinal hemorrhage syndrome
DNM2
Autosomal dominant Charcot-Marie-Tooth disease type 2M



Fetal akinesia-cerebral and retinal hemorrhage syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2M

Synonym(s):
(no synonyms)

Synonym(s):
- CMT2M
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: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.