CUI | Disease | Vocabulary | Name in Vocabulary | Code |
---|---|---|---|---|
C1854520 | SEBASTIAN SYNDROME | DO | MYH-9 related disease | 0060651 |
C1854520 | SEBASTIAN SYNDROME | MONDO | May-Hegglin anomaly | 0007954 |
C1854520 | SEBASTIAN SYNDROME | MONDO | Sebastian syndrome | 0011526 |
C1854520 | SEBASTIAN SYNDROME | MONDO | MYH-9 related disease | 0015912 |
C1854520 | SEBASTIAN SYNDROME | MSH | MYH9-Related Disorders | C535507 |
C1854520 | SEBASTIAN SYNDROME | MSH | Sebastian syndrome | C535507 |
C1854520 | SEBASTIAN SYNDROME | MSH | Deafness, Autosomal Dominant 17 | C535507 |
C1854520 | SEBASTIAN SYNDROME | NCI | Sebastian Syndrome | C131650 |
C1854520 | SEBASTIAN SYNDROME | OMIM | MAY-HEGGLIN ANOMALY | 155100 |
C1854520 | SEBASTIAN SYNDROME | OMIM | MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS | 155100 |
C1854520 | SEBASTIAN SYNDROME | OMIM | EPSTEIN SYNDROME | 155100 |
C1854520 | SEBASTIAN SYNDROME | OMIM | FECHTNER SYNDROME | 155100 |
C1854520 | SEBASTIAN SYNDROME | OMIM | GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA | 155100 |
C1854520 | SEBASTIAN SYNDROME | OMIM | SEBASTIAN SYNDROME | 155100 |
C1854520 | SEBASTIAN SYNDROME | ORDO | Epstein syndrome | 1019 |
C1854520 | SEBASTIAN SYNDROME | ORDO | MYH9-related disease | 182050 |
C1854520 | SEBASTIAN SYNDROME | ORDO | Sebastian syndrome | 807 |
C1854520 | SEBASTIAN SYNDROME | ORDO | May-Hegglin thrombocytopenia | 850 |