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Childhood-onset nemaline myopathy
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant Charcot-Marie-Tooth disease type 2F
1 OMIM reference -
1 associated gene
No signs/symptoms info
Childhood-onset nemaline myopathy
Autosomal dominant Charcot-Marie-Tooth disease type 2F

ACTA1
(UniProt - OMIM)
 HSPB1
(UniProt - OMIM)
KBTBD13
(UniProt - OMIM)
KLHL41
(UniProt - OMIM)
NEB
(UniProt - OMIM)
TPM2
(UniProt - OMIM)
TPM3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TPM3
(0.49)
HSPB1


Citations in the biomedical literature:


Childhood-onset nemaline myopathy
ACTA1 KBTBD13 KLHL41 NEB TPM2 TPM3

Autosomal dominant Charcot-Marie-Tooth disease type 2F
HSPB1



Childhood-onset nemaline myopathy
Autosomal dominant Charcot-Marie-Tooth disease type 2F

Synonym(s):
- Mild nemaline myopathy
Synonym(s):
- CMT2F
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.