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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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male internal pseudohermaphroditism
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C536665 |
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idiopathic intestinal pseudoobstruction
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C566502 |
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congenital, autosomal recessive fibrosis of extraocular muscles
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C566587 |
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congenital bilateral recurrent nerve paralysis and ptosis
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8665 |
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valve incompetence, pulmonary
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D011665 |
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valve insufficiency, pulmonary
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D011665 |
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valve regurgitation, pulmonary
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D011665 |
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myopia, and sensorineural deafness spondyloepiphyseal dysplasia
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C566659 |
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ectodermal dysplasia, pure hair-nail type
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C566592 |
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iliopsoas abscess, pyogenic
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D016659 |
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iliopsoas abscesses, pyogenic
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D016659 |
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chromosome 5 ring
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16654 |
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spondyloepimetaphyseal dysplasia, shohat type
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C566523 |
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Hodgkin's nodular sclerosis
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4665 |
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SEMD, shohat type
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C566523 |
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