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 )
- is a type of
-
- disjoint_from
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models