|
type IV, mucopolysaccharidosis
|
D009085 |
|
|
type IVs, mucopolysaccharidosis
|
D009085 |
|
|
type 6, mucopolysaccharidosis
|
D009087 |
|
|
type VI, mucopolysaccharidosis
|
D009087 |
|
|
rutledge lethal multiple congenital anomaly syndrome
|
D019082 |
|
|
syndromic X-linked mental retardation 35
|
30908 |
|
|
deafness and myopia syndrome
|
9082 |
|
|
deafness and myopia; DFNMYP
|
http://purl.obolibrary.org/obo/MONDO_0009082 |
|
|
sulfatase deficiencies, n-acetylglucosamine-6-sulfate
|
D009084 |
|
|
sulfatase deficiency, n-acetylglucosamine-6-sulfate
|
D009084 |
|
|
deficiencies, Acetyl-CoA:alpha-Glucosaminide n-acetyltransferase
|
D009084 |
|
|
deficiency, Acetyl-CoA:alpha-Glucosaminide n-acetyltransferase
|
D009084 |
|
|
deficiencies, glycoprotein neuraminidase
|
D009081 |
|
|
familial congenital moderate neural hearing loss
|
9083 |
|
