|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of anemia characterized by an normal concentration of hemoglobin in the erythrocytes and lower than normal size of the erythrocytes. (Human Phenotype Ontology, HP_0004856)|
|Downloads & Tools|
1 genes associated with the normochromic microcytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|DNAJC19||DnaJ (Hsp40) homolog, subfamily C, member 19|