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 |