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
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 13160.0
XPNPEP3 nephronophthisis (disease) 13163
nephronophthisis-like nephropathy 1 13163
parkinson disease 16 13167
Parkinson disease 16; PARK16 http://purl.obolibrary.org/obo/MONDO_0013167
Alzheimer disease 19 14316
cerebellum astrocytoma (excluding glioblastoma) 3165
diencephalon astrocytoma (excluding glioblastoma) 3169
muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2 13162
muscular dystrophy-dystroglycanopathy (limb-girdle) type C3 13161
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2 13162
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2; MDDGC2 http://purl.obolibrary.org/obo/MONDO_0013162
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3 13161
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3; MDDGC3 http://purl.obolibrary.org/obo/MONDO_0013161
Alzheimer's disease 19 14316