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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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malignant renal neoplasm
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2367 |
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benign axillary neoplasm
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36781 |
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uniparental disomy of 21
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C536794 |
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uniparental disomy of 22
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C536796 |
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plasma-membrane, deficiency of carnitine transporter
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C536778 |
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diffuse corticomeningeal, of divry and van bogaert angiomatosis
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C536367 |
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woods black norbury syndrome
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C536743 |
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familial, with nocturnal wandering and ictal fear epilepsy
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C563679 |
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spastic ataxia of charlevoix-saguenay
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C536787 |
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short stature, obesity and hypogonadism Sex-linked mental retardation
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C536715 |
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glaucoma (disease) of childhood
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20367 |
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uniparental disomy of chromosome 21
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C536794 |
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malignant neoplasm of the kidney
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2367 |
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SBBYS variant of ohdo syndrome
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C536717 |
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say-barber-biesecker-young-simpson variant of ohdo syndrome
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C536717 |
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