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
syndrome, chemke D058494
syndrome, fukuyama D058494
syndrome, pagon D058494
syndrome, walker-warburg D058494
syndrome, warburg D058494
walker-warburg syndrome D058494
warburg syndrome D058494
limb-girdle, autosomal recessive, with mental retardation muscular dystrophy D058494
limb-girdle, type 2k muscular dystrophy D058494
muscular dystrophy, limb-girdle, autosomal recessive, with mental retardation D058494
muscular dystrophy, limb-girdle, type 2k D058494
type a, 1 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) D058494
type c, 1 muscular dystrophy-dystroglycanopathy (limb-girdle) D058494
fukuyama type cerebromuscular dystrophy D058494
POMT1-Related muscle-eye-brain disease D058494