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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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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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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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progressive tubulointerstitial, with cholestatic liver disease nephropathy
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C566573 |
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type IE usher syndrome
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C566577 |
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type IF usher syndrome
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C566586 |
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hystrix-like ichthyosis with deafness
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C566528 |
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SCPx-Deficient leukoencephalopathy with dystonia and motor neuropathy
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C566654 |
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infra-auricular cutaneous, with tall stature and advanced bone age creases
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C566543 |
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