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5 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Periventricular nodular heterotopia
Progeria-associated arthropathy

ARFGEF2 LMNA
ERMARD
FLNA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FLNA
(0.73)
LMNA



Citations in the biomedical literature:


Periventricular nodular heterotopia
ARFGEF2 ERMARD FLNA
Progeria-associated arthropathy
LMNA



Periventricular nodular heterotopia
Progeria-associated arthropathy

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

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

External references:
5 OMIM references -
1 MeSH reference: D054091
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.