CUI | Disease | Vocabulary | Name in Vocabulary | Code |
---|---|---|---|---|
C0020725 | Type II Mucolipidosis | DO | inclusion-cell disease | 0080070 |
C0020725 | Type II Mucolipidosis | HPO | Deficiency of N-acetylglucosamine-1-phosphotransferase | HP:0003264 |
C0020725 | Type II Mucolipidosis | MONDO | mucolipidosis type II | 0009650 |
C0020725 | Type II Mucolipidosis | MSH | Type II Mucolipidosis | D009081 |
C0020725 | Type II Mucolipidosis | MSH | Lipomucopolysaccharidosis | D009081 |
C0020725 | Type II Mucolipidosis | MSH | Mucolipidoses | D009081 |
C0020725 | Type II Mucolipidosis | MSH | Pseudo-Hurler Polydystrophy | D009081 |
C0020725 | Type II Mucolipidosis | MSH | Mucolipidosis Type IV | D009081 |
C0020725 | Type II Mucolipidosis | MSH | Type I Mucolipidosis | D009081 |
C0020725 | Type II Mucolipidosis | NCI | Mucolipidosis Type II | C61270 |
C0020725 | Type II Mucolipidosis | NCI | Inclusion-cell Disease | C61270 |
C0020725 | Type II Mucolipidosis | NCI | I-Cell Disease | C61270 |
C0020725 | Type II Mucolipidosis | OMIM | I-CELL DISEASE | 252500 |
C0020725 | Type II Mucolipidosis | OMIM | MUCOLIPIDOSIS II ALPHA/BETA | 252500 |
C0020725 | Type II Mucolipidosis | ORDO | Mucolipidosis type II | 576 |