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Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Estrogen resistance syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
Estrogen resistance syndrome

DNM1L
(UniProt - OMIM)
 ESR1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DNM1L
(0.86)
ESR1


Citations in the biomedical literature:


Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
DNM1L
Estrogen resistance syndrome
ESR1



Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
Estrogen resistance syndrome

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
(no data available)
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
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.