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Summary Literature (0)
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:

Xenbase Genes : colec11

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009927 - 3MC syndrome 2

MIM:
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)