Search Ontology:
Human Disease

autosomal genetic disease

Term ID
DOID:0050739
Synonyms
Definition
A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes. (2)
References
Ontology
Human Disease   ( DOID:0050739 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models