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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 1e
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C566589 |
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congenital, 2 fibrosis of extraocular muscles
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C566587 |
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chromosome 8p23.1 deletion
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16658 |
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8p23.1 microdeletion syndrome
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16658 |
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polymicrogyria, bilateral perisylvian
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C536658 |
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congenital bilateral perisylvian syndrome
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C536658 |
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congenital, autosomal recessive fibrosis of extraocular muscles
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C566587 |
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type a2 postaxial polydactyly
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C566585 |
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polydactyly, postaxial, type a2
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C566585 |
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postaxial polydactyly, type a2
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C566585 |
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type IF usher syndrome
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C566586 |
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familial broad terminal phalanges
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C566588 |
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usher syndrome, type IF
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C566586 |
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