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
Bothnia retinal dystrophy http://purl.obolibrary.org/obo/MONDO_0011838
Västerbotten dystrophy http://purl.obolibrary.org/obo/MONDO_0011838
Vasterbotten dystrophy http://purl.obolibrary.org/obo/MONDO_0011838
Newfoundland cone-rod dystrophy http://purl.obolibrary.org/obo/MONDO_0011839
Newfoundland ROD-cone dystrophy; NFRCD http://purl.obolibrary.org/obo/MONDO_0011839
NFRCD http://purl.obolibrary.org/obo/MONDO_0011839
RLBP1 cone-rod dystrophy http://purl.obolibrary.org/obo/MONDO_0011839
Newfoundland ROD-cone dystrophy http://purl.obolibrary.org/obo/MONDO_0011839
cone-rod dystrophy caused by mutation in RLBP1 http://purl.obolibrary.org/obo/MONDO_0011839
dilated cardiomyopathy 1M http://purl.obolibrary.org/obo/MONDO_0011840
dilated cardiomyopathy type 1M http://purl.obolibrary.org/obo/MONDO_0011840
cardiomyopathy, dilated, 1M http://purl.obolibrary.org/obo/MONDO_0011840
familial isolated dilated cardiomyopathy caused by mutation in CSRP3 http://purl.obolibrary.org/obo/MONDO_0011840
cardiomyopathy, dilated, type 1M http://purl.obolibrary.org/obo/MONDO_0011840
CMD1M http://purl.obolibrary.org/obo/MONDO_0011840
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