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
Ring chromosome 5 syndrome 16654
Mental Retardation, Autosomal Recessive 68 32665
cataract 33; CTRCT33 http://purl.obolibrary.org/obo/MONDO_0012665
autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation 14665
nodular sclerosis Classic Hodgkin lymphoma 4665
autosomal dominant Charcot-Marie-Tooth disease type 2V 14665
INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68 32665
nerve paralysis, Facial 5665
paralysis Of Facial nerve 5665
nodular sclerosis Hodgkin lymphoma 4665
nodular sclerosis Hodgkin's disease 4665
nodular sclerosis Hodgkin's lymphoma 4665
shohat type SEMD C566523
missouri type SEMD C566574
intellectual disability, X-linked, syndromic 6 10665