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
distal, early-onset, autosomal dominant myopathy D049310
dystrophic epidermolysis bullosa inversa 19310
granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type II 9310
granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type II; CDG2 http://purl.obolibrary.org/obo/MONDO_0009310
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2 9310
granulomatous disease, chronic, due to Ncf2 deficiency 9310
recessive dystrophic epidermolysis bullosa inversa 19310
inverse recessive dystrophic epidermolysis bullosa 19310
distal muscular dystrophies D049310
tibial muscular dystrophies D049310
finnish-markesbery muscular dystrophy D049310
udd-markesbery muscular dystrophy D049310
muscular dystrophies, distal D049310
muscular dystrophy, distal D049310
myopathy 1, distal D049310