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DO Term : 3MC syndrome 1 [DOID:0060575] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
OMIM:257920,
257920

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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