| Label | Id | |
|---|---|---|
| neuronal, type 2b charcot-marie-tooth disease | C537989 | |
| MRKH, type 2 | 10989 | |
| non-distal trisomy 9q | 19890 | |
| non-telomeric trisomy 9q | 19890 | |
| periapical dental abscess | 6989 | |
| HEMOGLOBIN F DIS | 20989 | |
| Hemoglobin F Disease | 20989 | |
| distal deletion 4q | 19895 | |
| distal monosomy 4q | 19895 | |
| telomeric deletion 4q | 19895 | |
| spermatogenic failure 53 | 30989 | |
| fibrous histiocytoma NOS (morphologic abnormality) | 2989 | |
| HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN | http://purl.obolibrary.org/obo/MONDO_0020989 | |
| polycythemia vera; PV | http://purl.obolibrary.org/obo/MONDO_0009891 | |
| Disease, Hemoglobin F | 20989 |