Pectus Carinatum

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Pectus Carinatum is related to spondyloepimetaphyseal dysplasia, strudwick type and brittle bone disorder. An important gene associated with Pectus Carinatum is FBN1 (Fibrillin 1), and among its related pathways/superpathways are Phospholipase-C Pathway and Pathways affected in adenoid cystic carcinoma. Affiliated tissues include breast and heart, and related phenotypes are growth/size/body region and limbs/digits/tail

Related ID：

MALACARDS：PCT001