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
CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT 26782
chondrodysplasia punctata 2, X-linked dominant 26782
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 71 32678
Glutaminase Deficiency With Neonatal Epileptic Encephalopathy 32678
special senses disorder D012678
special senses disorders D012678
epileptic encephalopathy, early infantile, 71 32678
developmental and epileptic encephalopathy, 71 32678
atrial fibrillation, familial, 5 12678
atrial fibrillation, familial, 5; ATFB5 http://purl.obolibrary.org/obo/MONDO_0012678
childhood adult fibrosarcoma http://purl.obolibrary.org/obo/MONDO_0002678
pediatric adult fibrosarcoma http://purl.obolibrary.org/obo/MONDO_0002678
adult fibrosarcoma of childhood http://purl.obolibrary.org/obo/MONDO_0002678
senses disorder, special D012678
senses disorders, special D012678