Search Ontology:
Human Disease
3MC syndrome 1
- Term ID
- DOID:0060575
- Synonyms
-
- Definition
- A 3MC syndrome that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the mannan binding lectin serine peptidase 1 gene (MASP1) on chromosome 3q27. (2)
- References
- Ontology
- Human Disease ( DOID:0060575 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models