SYNONIMS: CFC syndrome ICD10 code: Q87.8 ORPHANET number: ORPHA1340 For more information about this disease, please visit the Orphanet website. Visitors from North America may also contact NIH Office of Rare Diseases Research website 0 FacebookTwitterLinkedinWhatsappEmail previous post Familial hypomagnesemia with hypercalciuria and nephrocalcinosis next post Huntigton disease Related Articles An Unknown Rare Disease in Bulgaria – Tarlov... 23/10/2020 Is a global shift beginning in the paradigm... 23/10/2020 Regulation (EC) № 141/2000 for orphan medicinal products... 22/10/2020 Hereditary retinal dystrophies 21/10/2020 The Importance of Reference Centers and Registries for... 20/10/2020 European Reference Networks – Animation clip for patients... 19/10/2020 Challenges for patients with congenital adrenal hyperplasia and... 14/10/2020 Generation of FX -/- and Gmds -/- CHOZN... 12/10/2020 Natural history of multiple sulfatase deficiency: Retrospective phenotyping... 08/10/2020
