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
autosomal recessive limb-girdle muscular dystrophy type 2O 13161
muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT1-Related http://purl.obolibrary.org/obo/MONDO_0013161
muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT1-related 13161
muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-Related http://purl.obolibrary.org/obo/MONDO_0013162
muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-related 13162
muscular dystrophy, limb-girdle, type 2N 13162
muscular dystrophy, limb-girdle, type 2O 13161
Streptococcus infectious meningitis 1316
fatal post-viral neurodegenerative disorder 18316
cancer of minor salivary gland 21316
chromosome 2, monosomy 2q24 C538316
cauda equina neoplasm 3164
cauda equina neoplasm (disease) 3164
Cauda equina neoplasms 3164
maculopapular cutaneous mastocytosis 19316