MONDO Find_IDs Find_Terms Annotation
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created at 2019-07-11 18:15:35 UTC
updated at 2020-12-23 10:47:34 UTC
diseases or disorders as defined in MONDO disease ontology (the version released on 2019-05-28). The terms are sourced from BioPortal on July 12, 2019.
121,242 entries

There is 0 pattern entry.

Label
Id
DSP arrhythmogenic right ventricular cardiomyopathy http://purl.obolibrary.org/obo/MONDO_0011831
autosomal dominant nonsyndromic deafness 44 http://purl.obolibrary.org/obo/MONDO_0011832
deafness, autosomal dominant 44 http://purl.obolibrary.org/obo/MONDO_0011832
CCDC50 autosomal dominant nonsyndromic deafness http://purl.obolibrary.org/obo/MONDO_0011832
autosomal dominant nonsyndromic deafness caused by mutation in CCDC50 http://purl.obolibrary.org/obo/MONDO_0011832
autosomal dominant deafness 44 http://purl.obolibrary.org/obo/MONDO_0011832
deafness, autosomal dominant type 44 http://purl.obolibrary.org/obo/MONDO_0011832
deafness, autosomal dominant 44; DFNA44 http://purl.obolibrary.org/obo/MONDO_0011832
autosomal dominant nonsyndromic deafness type 44 http://purl.obolibrary.org/obo/MONDO_0011832
DFNA44 http://purl.obolibrary.org/obo/MONDO_0011832
spinocerebellar ataxia type 21 http://purl.obolibrary.org/obo/MONDO_0011833
spinocerebellar ataxia 21; SCA21 http://purl.obolibrary.org/obo/MONDO_0011833
spinocerebellar ataxia 21 http://purl.obolibrary.org/obo/MONDO_0011833
spinocerebellar ataxia type 21 http://purl.obolibrary.org/obo/MONDO_0011833
SCA21 http://purl.obolibrary.org/obo/MONDO_0011833
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