|OBO ID: DOID:0060576|
|Term Name:||3MC syndrome 2||Search Ontology:|
|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. (2)|
|Ontology:||Human Disease (DOID:0060576)|
OTHER 3MC syndrome 2 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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