ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Autosomal dominant limb-girdle muscular dystrophy type 1C

Unclassified chronic myeloproliferative disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CAV3	(0.75)	PDGFRB

Citations in the biomedical literature:

Autosomal dominant limb-girdle muscular dystrophy type 1C		Unclassified chronic myeloproliferative disease
	Synonym(s): - LGMD1C - Limb-girdle muscular dystrophy due to caveolin-3 deficiency		Synonym(s): - CMPD-U - Undifferentiated myeloproliferative disease

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.