MONDO_merge Find_IDs Find_Terms Annotation
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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
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