ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Hereditary sensorimotor neuropathy with hyperelastic skin

Lethal arteriopathy syndrome due to FBLN4 deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FBLN5	(0.76)	EFEMP2

Citations in the biomedical literature:

Hereditary sensorimotor neuropathy with hyperelastic skin		Lethal arteriopathy syndrome due to FBLN4 deficiency

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare surgical thoracic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.