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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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watermelon stomach disease
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C538665 |
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rare genetic disease with myoclonus as a major feature
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17665.0 |
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paternal uniparental disomy of chromosome 1
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16650 |
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maternal uniparental disomy of chromosome 1
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16651 |
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paternal uniparental disomy of chromosome type 1
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16650 |
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maternal uniparental disomy of chromosome type 1
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16651 |
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intellectual developmental disorder, autosomal recessive 68
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32665 |
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peroxisome biogenesis disorder, complementation group e
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C566569 |
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deafness, autosomal dominant 78
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33665 |
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familial, autosomal dominant periodic fever
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C536657 |
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familial, autosomal dominant visceral neuropathy
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C566502 |
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extrahepatic bile duct adenocarcinoma
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2665 |
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persistent muellerian duct syndrome
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C536665 |
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persistent mullerian duct syndrome
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C536665 |
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persistent müllerian duct syndrome
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C536665 |
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