|OBO ID: DOID:0060575|
|Term Name:||3MC syndrome 1||Search Ontology:|
|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)|
|Ontology:||Human Disease (DOID:0060575)|
|is a type of:||
OTHER 3MC syndrome 1 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.