Search Ontology:
Human Disease

3MC syndrome 2

Term ID
DOID:0060576
Synonyms
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)
References
Ontology
Human Disease   ( DOID:0060576 )
Relationships
is a type of
disjoint_from
Other Pages
Genes Involved
Zebrafish Models
Citations