OBO ID: DOID:0060576
Term Name: 3MC syndrome 2 Search Ontology:
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 3MC syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
COLEC11 3MC syndrome 2 265050
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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