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
GJB3 autosomal dominant nonsyndromic deafness 12976
deafness, autosomal dominant type 2B 12976
deafness, autosomal dominant type 3B 12975
primary ciliary dyskinesia 11 without situs inversus 12978
primary ciliary dyskinesia 12 12979
primary ciliary dyskinesia 12 without situs inversus 12979
primary ciliary dyskinesia caused by mutation in RSPH4A 12978
primary ciliary dyskinesia caused by mutation in RSPH9 12979
primary ciliary dyskinesia type 11 12978
primary ciliary dyskinesia type 12 12979
epilepsy, nocturnal frontal lobe, 2 11297
deafness, autosomal dominant 2B 12976
deafness, autosomal dominant 2B; DFNA2B http://purl.obolibrary.org/obo/MONDO_0012976
deafness, autosomal dominant 3B; DFNA3B http://purl.obolibrary.org/obo/MONDO_0012975
deafness, autosomal dominant 59 12974