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| license |
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| created at |
2021-12-23 00:44:09 UTC |
| updated at |
2021-12-23 01:31:33 UTC |
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"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
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82,788 entries
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There is 0 pattern entry.
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limb-girdle, type 2k muscular dystrophy
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D058494 |
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muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1
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D058494 |
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muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1
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D058494 |
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muscle eye brain disease, POMT1 related
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D058494 |
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fukuyama type congenital muscular dystrophy
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D058494 |
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hydrocephalus, agyria, and retinal dysplasia
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D058494 |
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type a1 congenital muscular dystrophy dystroglycanopathy with brain and eye anomalies
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D058494 |
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type a1 congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies
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D058494 |
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muscular dystrophy, congenital, fukuyama type
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D058494 |
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fukuyama muscular dystrophy
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D058494 |
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POMT1-Related muscle-eye-brain disease
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D058494 |
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POMT1-Related muscle-eye-brain diseases
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D058494 |
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fukuyama type cerebromuscular dystrophy
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D058494 |
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muscular dystrophy due to defective glycosylation of dystroglycan 4a
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D058494 |
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congenital muscular dystrophy dystroglycanopathy with brain and eye anomalies, type a1
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D058494 |
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