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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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communication disorders, developmental
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D003147 |
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familial isolated dilated cardiomyopathy caused by mutation in NEXN
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13147 |
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inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive
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30314 |
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inflammatory bowel disease, early-onset, autosomal recessive
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30314 |
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acquired communication disorder
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D003147 |
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childhood communication disorder
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D003147 |
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developmental communication disorder
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D003147 |
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neurogenic communication disorder
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D003147 |
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acquired communication disorders
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D003147 |
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childhood communication disorders
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D003147 |
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developmental communication disorders
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D003147 |
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neurogenic communication disorders
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D003147 |
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fetal brain disruption sequence
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23142 |
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TUBB1 autosomal dominant macrothrombocytopenia
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13141 |
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emery-dreifuss, autosomal dominant muscular dystrophy
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D000083144 |
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