Search Ontology:
Human Disease

autosomal recessive disease

Term ID
DOID:0050737
Synonyms
Definition
An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop. (2)
References
Ontology
Human Disease   ( DOID:0050737 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models