ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Annular epidermolytic ichthyosis

Familial renal amyloidosis due to Apolipoprotein AI variant

KRT1	(UniProt - OMIM)		APOA1	(UniProt - OMIM)
KRT10	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT1	(0.72)	APOA1

Citations in the biomedical literature:

Annular epidermolytic ichthyosis		Familial renal amyloidosis due to Apolipoprotein AI variant
	Synonym(s): - AEI		Synonym(s): - Apolipoprotein AI amyloidosis - Familial amyloid nephropathy due to apolipoprotein AI variant - Hereditary amyloid nephropathy due to apolipoprotein AI variant - Hereditary renal amyloidosis due to apolipoprotein AI variant

	Classification (Orphanet): - Rare genetic disease - Rare skin 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 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.