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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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muscular dystrophy, limb-girdle, type 2k
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D058494 |
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walker warburg syndrome, fktn related
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D058494 |
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agyria, and retinal dysplasia hydrocephalus
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D058494 |
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fktn-related walker-warburg syndromes
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D058494 |
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POMT1 related muscle eye brain disease
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D058494 |
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disease, POMT1-Related muscle-eye-brain
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D058494 |
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dystrophy, fukuyama muscular
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D058494 |
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fukuyama congenital muscular dystrophy
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D058494 |
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limb-girdle, autosomal recessive, with mental retardation muscular dystrophy
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D058494 |
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congenital, fukuyama type muscular dystrophy
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D058494 |
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COD MD syndrome
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D058494 |
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MEB (muscle-eye-brain) syndrome
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D058494 |
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fktn-related walker-warburg syndrome
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D058494 |
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walker warburg syndrome
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D058494 |
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fktn related walker warburg syndrome
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D058494 |
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