aspartylglucosaminuria

As nouns the difference between aspartylglucosaminidase and aspartylglucosaminuria

is that aspartylglucosaminidase is a human gene and amidohydrolase enzyme involved in the catabolism of n-linked oligosaccharides of glycoproteins while aspartylglucosaminuria is a rare autosomal-recessive lysosomal storage disorder caused by deficient activity of the enzyme aspartylglucosaminidase.

As a verb enzyme

is .

As a noun aspartylglucosaminuria is

a rare autosomal-recessive lysosomal storage disorder caused by deficient activity of the enzyme aspartylglucosaminidase.

As nouns the difference between disorder and aspartylglucosaminuria

is that disorder is absence of order; state of not being arranged in an orderly manner while aspartylglucosaminuria is a rare autosomal-recessive lysosomal storage disorder caused by deficient activity of the enzyme aspartylglucosaminidase.

As an adjective lysosomal

is of, pertaining to, or originating in lysosomes.

As a noun aspartylglucosaminuria is

a rare autosomal-recessive lysosomal storage disorder caused by deficient activity of the enzyme aspartylglucosaminidase.

As an adjective recessive

is .

As a noun aspartylglucosaminuria is

a rare autosomal-recessive lysosomal storage disorder caused by deficient activity of the enzyme aspartylglucosaminidase.

As an adjective autosomal

is of or pertaining to autosomes.

As a noun aspartylglucosaminuria is

a rare autosomal-recessive lysosomal storage disorder caused by deficient activity of the enzyme aspartylglucosaminidase.

Aspartylglycosaminuria is an alternative form of aspartylglucosaminuria.

As nouns the difference between aspartylglycosaminuria and aspartylglucosaminuria

is that aspartylglycosaminuria is while aspartylglucosaminuria is a rare autosomal-recessive lysosomal storage disorder caused by deficient activity of the enzyme aspartylglucosaminidase.