MONDO_merge Find_IDs Find_Terms Annotation
manager
language -
license -
created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
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