Given below are two statements:
Statement I: Alkaptonuria is known as an inborn error of metabolism associated with certain amino acids
Statement II: The mutation of homogentisate 1,2-dioxygenase (HGD) gene leads to abnormal metabolism of certain amino acids like phenylalanine and tyrosine that leads to alkaptonuria
In the light of the above statements, choose the most appropriate answer from the options given below