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DOID:0060576 - 3MC syndrome 2
Disease 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.
Synonyms:
Echinobase Genes

MIM:265050 - 3mc syndrome 2; 3mc2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
3MC syndrome (is_a)