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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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limb-girdle, type 2k muscular dystrophy
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D058494 |
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type a, 1 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
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D058494 |
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type c, 1 muscular dystrophy-dystroglycanopathy (limb-girdle)
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D058494 |
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muscle-eye-brain disease, POMT1-Related
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D058494 |
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muscle-eye-brain diseases, POMT1-Related
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D058494 |
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walker-warburg syndrome, fktn-related
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D058494 |
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fukuyama type congenital muscular dystrophy
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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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microcephaly-short stature-intellectual disability-facial dysmorphism syndrome
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18494 |
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muscle eye brain disease, POMT1 related
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D058494 |
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fukuyama type cerebromuscular 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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muscular dystrophy due to defective glycosylation of dystroglycan 4a
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D058494 |
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