ODCs

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

PROTEIN INTERACTIONS: 1

5 OMIM references -
4 associated genes
No signs/symptoms info

Autosomal dominant limb-girdle muscular dystrophy type 1B

Familial hemophagocytic lymphohistiocytosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LMNA	(0.63)	UNC13D

Citations in the biomedical literature:

Autosomal dominant limb-girdle muscular dystrophy type 1B		Familial hemophagocytic lymphohistiocytosis
	Synonym(s): - LGMD1B - Limb-girdle muscular dystrophy due to lamin A/C deficiency		Synonym(s): - Familial HLH

	Classification (Orphanet): - Rare cardiac disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare immune disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 5 OMIM references - No MeSH references

No signs/symptoms info available.