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
primary ciliary dyskinesia type 11 12978
deafness, autosomal dominant 3B; DFNA3B http://purl.obolibrary.org/obo/MONDO_0012975
primary ciliary dyskinesia type 12 12979
cleidocranial digital dysostoses D002973
deafness, autosomal dominant 59 12974
deafness, autosomal dominant 59; DFNA59 http://purl.obolibrary.org/obo/MONDO_0012974
cleidocranial digital dysostosis D002973
diaphragmatic hernia exomphalos corpus callosum agenesis 22977
limb-girdle muscular dystrophy type 1H 13297
Herpesviridae infectious embryofetopathy 42971
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 100297
trichoepithelioma, multiple familial, 1 42977
febrile seizures, familial, 10 12972
febrile seizures, familial, 10; FEB10 http://purl.obolibrary.org/obo/MONDO_0012972
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1 100297