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 |