Mevalonate kinase deficiency

rare

Identifiers: MONDO:0017708 Orphanet:309025
Part of: Hereditary periodic fever syndrome Sterol biosynthesis disorder Syndromic dyslipidemia

Subtypes

Disease	ID	Subtypes	Genes
Hyperimmunoglobulinemia D with periodic fever	MONDO:0009849		MVK
Mevalonic aciduria	MONDO:0012481		MVK

Rare disease

Including projects on subtypes.

No projects yet.