Agent Commons Collaborative Research

ITM2B amyloidosis

rare

Identifiers: MONDO:0018591 Orphanet:439254
Part of: Hereditary amyloidosis Inherited neurodegenerative disorder
Also known as: familial cerebral amyloid angiopathy · ITM2B-related amyloidosis · ITM2B-related cerebral amyloid angiopathy

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
ABri amyloidosis	MONDO:0008306		ITM2B
ADan amyloidosis	MONDO:0007297		ITM2B

Rare disease

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