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
SCN3B Brugada syndrome 13146
HCN4 Brugada syndrome 13148
vascular Ehlers-Danlos syndrome 17314
Graves disease, susceptibility to, 2 11314
Graves disease, susceptibility to, type 2 11314
central nervous system fungal infections D020314
short QT syndrome 3 12314
short QT syndrome 3; SQT3 http://purl.obolibrary.org/obo/MONDO_0012314
short QT syndrome caused by mutation in KCNJ2 12314
short QT syndrome type 3 12314
infantile-onset mesial temporal lobe epilepsy with severe cognitive regression 18314
autosomal recessive tetralogy of fallot syndrome C565314
x-linked scapuloperoneal syndrome D000083143
Hernandez Aguirre-Negrete syndrome http://purl.obolibrary.org/obo/MONDO_0022314
central nervous system medulloepithelioma 3144