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

Congenital alpha2 antiplasmin deficiency

Ligneous conjunctivitis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SERPINF2	(0.89)	PLG

Citations in the biomedical literature:

Congenital alpha2 antiplasmin deficiency		Ligneous conjunctivitis
	Synonym(s): (no synonyms)		Synonym(s): - Conjunctivitis lignosa

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

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Diseases of the eye and adnexa -

	Epidemiological data: (no data available)		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 - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.