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Supravalvular aortic stenosis

1 OMIM reference -
1 associated gene
1 sign/symptom

PROTEIN INTERACTIONS: 1

Familial renal amyloidosis due to lysozyme variant

1 associated gene
No signs/symptoms info

Supravalvular aortic stenosis

Familial renal amyloidosis due to lysozyme variant

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ELN	(0.52)	LYZ

Citations in the biomedical literature:

Supravalvular aortic stenosis		Familial renal amyloidosis due to lysozyme variant
	Synonym(s): - SVAS - Supravalvar aortic stenosis		Synonym(s): - Familial amyloid nephropathy due to lysozyme variant - Hereditary amyloid nephropathy due to lysozyme variant - Hereditary renal amyloidosis due to lysozyme variant - Lysozyme amyloidosis

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare surgical cardiac disease		Classification (Orphanet): - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: variable Average age of death: no data available Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: D021921		External references: No OMIM references No MeSH references

Supravalvular aortic stenosis
	Very frequent - Cardiac rhythm disorder / arrhythmia
Familial renal amyloidosis due to lysozyme variant
(no data available)