| CUI | Disease | Vocabulary | Name in Vocabulary | Code |
|---|---|---|---|---|
| C0340978 | May-Hegglin anomaly | DO | MYH-9 related disease | 0060651 |
| C0340978 | May-Hegglin anomaly | DO | Chediak-Higashi syndrome | 2935 |
| C0340978 | May-Hegglin anomaly | EFO | macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss | 0009646 |
| C0340978 | May-Hegglin anomaly | ICD10CM | Hereditary leukomelanopathy | D72.0 |
| C0340978 | May-Hegglin anomaly | ICD10CM | May-Hegglin syndrome | D72.0 |
| C0340978 | May-Hegglin anomaly | MONDO | May-Hegglin anomaly | 0007954 |
| C0340978 | May-Hegglin anomaly | MONDO | MYH-9 related disease | 0015912 |
| C0340978 | May-Hegglin anomaly | NCI | May-Hegglin Anomaly | C131646 |
| C0340978 | May-Hegglin anomaly | OMIM | MAY-HEGGLIN ANOMALY | 155100 |
| C0340978 | May-Hegglin anomaly | OMIM | MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS | 155100 |
| C0340978 | May-Hegglin anomaly | OMIM | EPSTEIN SYNDROME | 155100 |
| C0340978 | May-Hegglin anomaly | OMIM | FECHTNER SYNDROME | 155100 |
| C0340978 | May-Hegglin anomaly | OMIM | GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA | 155100 |
| C0340978 | May-Hegglin anomaly | OMIM | SEBASTIAN SYNDROME | 155100 |
| C0340978 | May-Hegglin anomaly | ORDO | MYH9-related disease | 182050 |
| C0340978 | May-Hegglin anomaly | ORDO | May-Hegglin thrombocytopenia | 850 |