ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

3 OMIM references -
3 associated genes
No signs/symptoms info

Autosomal recessive limb-girdle muscular dystrophy type 2G

Distal hereditary motor neuropathy type 2


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TCAP	(0.63)	HSPB3

Citations in the biomedical literature:

Autosomal recessive limb-girdle muscular dystrophy type 2G		Distal hereditary motor neuropathy type 2
	Synonym(s): - LGMD2G - Limb girdle muscular dystrophy due to telethonin deficiency		Synonym(s): - Distal spinal muscular atrophy type 2 - dHMN2 - dSMA2

	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: no data available Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.