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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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congenital, with synergistic divergence fibrosis of extraocular muscles
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C566508 |
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focal adult-onset torsion dystonia
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C566572 |
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primary adult-onset torsion dystonia
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C566572 |
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polydactyly, postaxial, type a2
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C566585 |
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bartter syndrome, type 4a
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C566530 |
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usher syndrome, type IE
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C566577 |
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usher syndrome, type IF
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C566586 |
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SEMD, shohat type
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C566523 |
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SEMD, missouri type
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C566574 |
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postaxial polydactyly, type a2
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C566585 |
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pure hair-nail type ectodermal dysplasia
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C566592 |
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congenital, megaconial type muscular dystrophy
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C566527 |
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type IE usher syndrome
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C566577 |
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hystrix-like ichthyosis with deafness
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C566528 |
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type IF usher syndrome
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C566586 |
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