OBO ID: DOID:0060575
Term Name: 3MC syndrome 1 Search Ontology:
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 )
Relationships
is a type of:
OTHER 3MC syndrome 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MASP1 3MC syndrome 1 257920
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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