ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Synpolydactyly type 2

Familial renal amyloidosis due to Apolipoprotein AI variant


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FBLN1	(0.63)	APOA1

Citations in the biomedical literature:

Synpolydactyly type 2		Familial renal amyloidosis due to Apolipoprotein AI variant
	Synonym(s): - SD2, Debeer type - SD2b - SPD, Debeer type - SPD2 - Synpolydactyly, Debeer type		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 bone disease - Rare developmental defect during embryogenesis - Rare genetic 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: (no data available)		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.