ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Familial encephalopathy with neuroserpin inclusion bodies

Ligneous conjunctivitis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SERPINI1	(0.52)	PLG

Citations in the biomedical literature:

Familial encephalopathy with neuroserpin inclusion bodies		Ligneous conjunctivitis
	Synonym(s): - FENIB		Synonym(s): - Conjunctivitis lignosa

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the eye and adnexa -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: any age Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - 1 MeSH reference: C536841		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.