ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
2 signs/symptoms

Congenital high-molecular-weight kininogen deficiency

Hereditary hyperferritinemia with congenital cataracts


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KNG1	(0.82)	FTL

Citations in the biomedical literature:

Congenital high-molecular-weight kininogen deficiency		Hereditary hyperferritinemia with congenital cataracts
	Synonym(s): (no synonyms)		Synonym(s): - Bonneau-Beaumont syndrome - HHCS - Hereditary hyperferritinemia-cataract syndrome

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

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C538137

Hereditary hyperferritinemia with congenital cataracts
	Very frequent - Cataract / lens opacification - Metabolic anomalies
Congenital high-molecular-weight kininogen deficiency
(no data available)