Caffey Disease (CAFYD)

Alias:

Infantile Cortical Hyperostosis

Cortical Congenital Hyperostosis

Cafyd

Hyperostosis, Cortical, Congenital

Hyperostosis Cortical Infantile

Caffey-Silverman Syndrome

De Toni-Caffey Disease

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Caffey Disease, also known as infantile cortical hyperostosis, is related to blood group, p1pk system and ehlers-danlos syndrome. An important gene associated with Caffey Disease is COL1A1 (Collagen Type I Alpha 1 Chain), and among its related pathways/superpathways are Phospholipase-C Pathway and Signaling by Receptor Tyrosine Kinases. Affiliated tissues include bone and skin, and related phenotypes are cellulitis and cortical irregularity

Related ID：

MALACARDS：CFF003

OMIM：114000

MESH：D006958