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
growth retardation, cataract, hearing loss, and unusual appearance microcephaly C567849
syndrome, CACH VWM D056784
myopathy, myofibrillar, bag3-related C567843
diffusa, myelinosis centralis D056784
diffusas, myelinosis centralis D056784
Vitamin K deficiency bleeding in newborn http://purl.obolibrary.org/obo/MONDO_0006784
emmonsia crescens infection C000656784
myelinosis centralis diffusas D056784
white matter diseases D056784
white matter disease D056784
global cerebral hypomyelination C567847
centralis diffusa, myelinosis D056784
cystic, without megalencephaly leukoencephalopathy C567845
myofibrillar, bag3-related myopathy C567843
hemorrhagic disease of newborn 6784