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
ARMD2 7932
x-linked opitz GBBB syndrome C567932
opitz syndrome C567932
maculopathy, age-related, 2 7932
macular Degeneration, Senile 7932
age related macular degeneration 2 7932
macular degeneration, age-related, 2 7932
macular degeneration, age-related, 2; ARMD2 http://purl.obolibrary.org/obo/MONDO_0007932
macular Degeneration, age-related, type 2 7932
mfm, filamin c-related C537932
myofibrillar, filamin c-related myopathy C537932
myofibrillar myopathy, filamin C-related C537932
myopathy, myofibrillar, filamin c-related C537932
autosomal dominant filaminopathy C537932
age related macular degeneration type 2 7932