FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term 3MC syndrome 2 ID (Ontology) DOID:0060576 (Human Disease)
Definition A 3MC syndrome that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the collectin subfamily member 11 gene (COLEC11) on chromosome 2p25.
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 Genes
 3MC syndrome 2       1
 for disease ribbon | 3MC syndrome 2       1
 model of | 3MC syndrome 2       1
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autosomal recessive disease__
syndrome_____________________|
                             3MC syndrome
                              |__3MC syndrome 2  1 rec.
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MIM:265050