MONDO Find_IDs Find_Terms Annotation
manager
language -
license -
created at 2019-07-11 18:15:35 UTC
updated at 2025-12-23 18:38:35 UTC
Diseases and disorders as defined in the MONDO ontology, the version 2025-01-07.
Only the terms under the node "disease" (MONDO_0000001) are included.

All identifiers use the CURIE format with the MONDO: prefix (e.g., MONDO:12345),
which corresponds to the full IRI namespace http://purl.obolibrary.org/obo/MONDO_.
112,359 entries
Label
Id
choroidal dystrophy, central areolar 2 MONDO:0013137
CACD2 MONDO:0013137
macular dystrophy, progressive MONDO:0013137
PRPH2 central areolar choroidal dystrophy MONDO:0013137
choroidal dystrophy, central areolar type 2 MONDO:0013137
central areolar choroidal dystrophy caused by mutation in PRPH2 MONDO:0013137
vertigo, benign recurrent, 2 MONDO:0013138
neutropenia, severe congenital, 2, autosomal dominant MONDO:0013139
GFI1 autosomal dominant severe congenital neutropenia MONDO:0013139
neutropenia, severe congenital 2, autosomal dominant MONDO:0013139
candidiasis, familial, 4 MONDO:0013140
candidiasis, familial chronic mucocutaneous MONDO:0013140
candidiasis, familial, 4, autosomal recessive MONDO:0013140
CLEC7A familial chronic mucocutaneous candidiasis MONDO:0013140
candidiasis, familial, type 4 MONDO:0013140