ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
6 signs/symptoms

Autosomal dominant limb-girdle muscular dystrophy type 1B

Melorheostosis with osteopoikilosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LMNA	(0.49)	LEMD3

Citations in the biomedical literature:

Autosomal dominant limb-girdle muscular dystrophy type 1B		Melorheostosis with osteopoikilosis
	Synonym(s): - LGMD1B - Limb-girdle muscular dystrophy due to lamin A/C deficiency		Synonym(s): - MSBD syndrome - Mixed sclerosing bone dystrophy

	Classification (Orphanet): - Rare cardiac disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -

	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: (no data available)

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

Melorheostosis with osteopoikilosis
	Very frequent - Cortical anomaly / thick bone cortical layer - Osteosclerosis / osteopetrosis / bone condensation Occasional - Capillary hemangioma / nevus / naevus flammeus / port-wine stain - Chronic arterial hypertension - Subcutaneous nodules / lipomas / tumefaction / swelling - Xanthomas / lipomas
Autosomal dominant limb-girdle muscular dystrophy type 1B
(no data available)