DISEASES

Disease-gene associations mined from literature

Human genes for hyperlysinemia

Hyperlysinemia [DOID:9274]

Hyperlysinemia is an autosomal recessive metabolic disorder characterized by an abnormal increase of lysine in the blood, but appears to be benign. It can be associated with saccharopine dehydrogenase.

Synonyms:  hyperlysinemia,  DOID:9274,  hyperlysinemia (disorder),  hyperlysinemia disorder,  hyperlysinemia

Linkouts:  OMIM #1 #2