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
myopathies, tubular aggregate D020914
intellectual disability, autosomal dominant 49 30914
mental retardation, autosomal dominant 49 30914
mental retardation, autosomal dominant 49; MRD49 http://purl.obolibrary.org/obo/MONDO_0030914
hypotrichosis-lymphedema-telangiectasia syndrome; HLTS http://purl.obolibrary.org/obo/MONDO_0011914
pediatric brainstem cancer 2914
myopathies, x-linked centronuclear D020914
acute intoxication by Blighia sapida 19140
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 914
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1; CADASIL1 http://purl.obolibrary.org/obo/MONDO_0000914
myopathy, x-linked centronuclear D020914
x linked centronuclear myopathy D020914
autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1 914
dystonic disorder caused by mutation in HPCA 9141
Sanchez Cascos cardioauditory syndrome 8914