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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
5 OMIM references -
4 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Familial hemophagocytic lymphohistiocytosis

LMNA PRF1
STX11
STXBP2
UNC13D


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Familial hemophagocytic lymphohistiocytosis
PRF1 STX11 STXBP2 UNC13D



Laminopathy type Decaudain-Vigouroux
Familial hemophagocytic lymphohistiocytosis

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

Synonym(s):
- Familial HLH

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

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

No signs/symptoms info available.