" /> Split-foot malformation with mesoaxial polydactyly - CISMeF





Preferred Label : Split-foot malformation with mesoaxial polydactyly;

Symbol : SFMMP;

CISMeF acronym : SFMMP;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the leucine zipper- and sterile alpha motif-containing kinase gene (ZAK, 609479.0001);

Prefixed ID : #616890;

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01/11/2024


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