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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease oculocutaneous albinism
Comorbidity C1858325|alpha-methylacyl-coa racemase deficiency
Sentences 1
PubMedID- 22987308 Incidental finding of alpha-methylacyl-coa racemase deficiency in a patient with oculocutaneous albinism type 4.

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