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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
6 signs/symptoms
Laminopathy type Decaudain-Vigouroux
Isolated osteopoikilosis

LMNA LEMD3


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Isolated osteopoikilosis
LEMD3



Laminopathy type Decaudain-Vigouroux
Isolated osteopoikilosis

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

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

Isolated osteopoikilosis

Very frequent
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Ectopic / horseshoe / fused kidneys
- Microcephaly
- Osteosclerosis / osteopetrosis / bone condensation
- Short stature / dwarfism / nanism
- Subcutaneous nodules / lipomas / tumefaction / swelling



Laminopathy type Decaudain-Vigouroux

(no data available)