ODCs

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

PROTEIN INTERACTIONS: 1

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

Autosomal recessive limb-girdle muscular dystrophy type 2G

Short stature - pituitary and cerebellar defects - small sella turcica


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TCAP	(0.63)	LHX4

Citations in the biomedical literature:

Autosomal recessive limb-girdle muscular dystrophy type 2G		Short stature - pituitary and cerebellar defects - small sella turcica
	Synonym(s): - LGMD2G - Limb girdle muscular dystrophy due to telethonin deficiency		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare endocrine disease - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): (no data available)

	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: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: no data available 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.