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 caused by mutation in POMGNT1 13161
autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMT2 13162
autosomal recessive limb-girdle muscular dystrophy type 2N 13162
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
hydrocephaly - low insertion umbilicus 43164
maculopapular cutaneous mastocytosis 19316
telangiectatic cutaneous mastocytosis 19316
Streptococcus infectious meningitis 1316
cancer of minor salivary gland 21316