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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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facial nerve palsy
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5665 |
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type a2 postaxial polydactyly
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C566585 |
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generalized lichenoid papular eruption
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15665 |
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facial nerve paralysis
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5665 |
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autosomal dominant parkinson disease 3
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C566552 |
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idiopathic intestinal pseudoobstruction
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C566502 |
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ectodermal dysplasia, pure hair-nail type
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C566592 |
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hypospadias, and penoscrotal inversion anal atresia
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C566526 |
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congenital, autosomal recessive fibrosis of extraocular muscles
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C566587 |
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familial broad terminal phalanges
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C566588 |
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shohat type spondyloepimetaphyseal dysplasia
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C566523 |
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missouri type spondyloepimetaphyseal dysplasia
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C566574 |
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intestinal, with secondary hypocalcemia hypomagnesemia
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C566593 |
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spondyloepimetaphyseal dysplasia, shohat type
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C566523 |
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congenital, with synergistic divergence fibrosis of extraocular muscles
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C566508 |
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