Search Ontology:
Human Disease

Rh deficiency syndrome

Term ID
DOID:0050641
Synonyms
Definition
A hemolytic anemia that is characterized by deficiency of Rh antigens, has_material_basis_in homozygous or compound heterozygous mutation in the RHAG gene on chromosome 6p12. (2)
References
Ontology
Human Disease   ( DOID:0050641 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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