| Label | Id | |
|---|---|---|
| telomeric deletion 4q | 19895 | |
| spermatogenic failure 53 | 30989 | |
| axonal, type 2b charcot-marie-tooth disease | C537989 | |
| neuronal, type 2b charcot-marie-tooth disease | C537989 | |
| non-distal duplication 9q | 19890 | |
| non-distal trisomy 9q | 19890 | |
| non-telomeric trisomy 9q | 19890 | |
| MRKH, type 2 | 10989 | |
| Disease, Hemoglobin F | 20989 | |
| breast cancer, NOS | 4989 | |
| Gillessen-Kaesbach-Nishimura syndrome; GIKANIS | http://purl.obolibrary.org/obo/MONDO_0009890 | |
| HPFH - Hereditary persistence of fetal hemoglobin | 20989 | |
| fibrous histiocytoma NOS (morphologic abnormality) | 2989 | |
| bedouin spastic ataxia syndrome | C536989 | |
| HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN | http://purl.obolibrary.org/obo/MONDO_0020989 |