|
Groll Hirschowitz syndrome
|
9086 |
|
|
deafness oligodontia syndrome
|
9089 |
|
|
deficiencies, n-acetylglucosamine-6-sulfate sulfatase
|
D009084 |
|
|
deficiency, n-acetylglucosamine-6-sulfate sulfatase
|
D009084 |
|
|
galactosamine 6 sulfatase deficiency
|
D009085 |
|
|
lethal acrodysgenital syndromes
|
D019082 |
|
|
lymph node syndrome, mucocutaneous
|
D009080 |
|
|
hereditary benign telangiectasia
|
C562908 |
|
|
carbohydrate-deficient glycoprotein syndrome, type II
|
8908 |
|
|
carbohydrate-deficient glycoprotein syndrome, type II, formerly
|
8908 |
|
|
carbohydrate-deficient glycoprotein syndrome, type II, formerly; CDGS2, formerly
|
8908 |
|
