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1 associated gene
6 signs/symptoms
PROTEIN INTERACTIONS: 1
4 OMIM references -
4 associated genes
No signs/symptoms info
Melorheostosis with osteopoikilosis
Autosomal dominant Emery-Dreifuss muscular dystrophy

LEMD3 LMNA
SYNE1
SYNE2
TMEM43


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Melorheostosis with osteopoikilosis
LEMD3
Autosomal dominant Emery-Dreifuss muscular dystrophy
LMNA SYNE1 SYNE2 TMEM43



Melorheostosis with osteopoikilosis
Autosomal dominant Emery-Dreifuss muscular dystrophy

Synonym(s):
- MSBD syndrome
- Mixed sclerosing bone dystrophy

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
4 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 Emery-Dreifuss muscular dystrophy

(no data available)