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
intellectual disability, autosomal dominant 39 14678
mental retardation, autosomal dominant 39 14678
mental retardation, autosomal dominant 39; MRD39 http://purl.obolibrary.org/obo/MONDO_0014678
intellectual disability, autosomal dominant type 39 14678
mental retardation, autosomal dominant type 39 14678
fungal skin disease 4678
chromosome 2P25.3 deletion syndrome 14678
MYT1L autosomal dominant non-syndromic intellectual disability 14678
fungal skin diseases 4678
autosomal dominant non-syndromic intellectual disability 39 14678
autosomal dominant non-syndromic intellectual disability caused by mutation in MYT1L 14678
anterior knee pain syndrome D046788
autosomal dominant intellectual disability 39 14678
pain syndrome, patellofemoral D046788
skin disease, fungal 4678