| Disease Aliases (34) | Cafyd Caffey de toni silvermann syndrome Caffey disease Caffey syndrome Caffey's disease, familial Caffey's disease Caffey-de toni-silvermann syndrome Congenital cortical hyperostoses Congenital cortical hyperostosis Congenital hyperostoses, cortical Congenital hyperostosis, cortical Cortical congenital hyperostoses Cortical congenital hyperostosis Cortical hyperostoses, congenital Cortical hyperostoses, infantile Cortical hyperostosis, congenital Cortical hyperostosis, infantile Disease, caffey Disease, familial caffey's Familial caffey disease Familial caffey's disease Familial caffeys disease Familial infantile cortical hyperostosis Hyperostoses, congenital cortical Hyperostoses, cortical congenital Hyperostoses, infantile cortical Hyperostosis, congenital cortical Hyperostosis, cortical congenital Hyperostosis, cortical, congenital Hyperostosis, infantile cortical Infantile cortical hyperostosis Infantile cortical hyperostoses P1pk blood group system, p(2) phenotype Syndrome, caffey-de toni-silvermann |
Associated Genes (1) NCBI-RefSeq: COL1A1 (Collagen type I alpha 1 chain) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Infantile cortical hyperostosis | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |