CUI | Disease | Vocabulary | Name in Vocabulary | Code |
---|---|---|---|---|
C1857761 | Alagille Syndrome 2 | DO | Alagille syndrome | 9245 |
C1857761 | Alagille Syndrome 2 | MONDO | Alagille syndrome due to a NOTCH2 point mutation | 0012439 |
C1857761 | Alagille Syndrome 2 | MSH | Alagille Syndrome | D016738 |
C1857761 | Alagille Syndrome 2 | MSH | Alagille Syndrome 2 | D016738 |
C1857761 | Alagille Syndrome 2 | MSH | Alagille Syndrome 1 | D016738 |
C1857761 | Alagille Syndrome 2 | MSH | Ductular Hypoplasia, Hepatic | D016738 |
C1857761 | Alagille Syndrome 2 | OMIM | ALAGILLE SYNDROME 2 | 610205 |
C1857761 | Alagille Syndrome 2 | ORDO | Alagille syndrome due to a NOTCH2 point mutation | 261629 |