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
x-linked opitz syndrome C567932
x-linked opitz syndrome (XLOS) C567932
macular Degeneration, Senile 7932
filamin c-related mfm C537932
muscular hypertrophy-hepatomegaly-polyhydramnios syndrome 17932
x-linked opitz GBBB syndrome C567932
age related macular degeneration 2 7932
age related macular degeneration type 2 7932
filamin C-related myofibrillar myopathy C537932
opitz GBBB syndrome, type i C567932
opitz GBBB syndrome, x-linked C567932
opitz-g syndrome, type i C567932
opitz syndrome, x-linked C567932