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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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thurston syndrome
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C557819 |
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OFDS XI
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C557821 |
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gabrielli syndrome
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C557821 |
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microdeletion 15q11.2
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C557830 |
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hypogammaglobulinemia, x-linked
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C562478 |
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x-linked hypogammaglobulinemia
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C562478 |
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ACACA deficiency
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C562678 |
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hypoparathyroidism, x-linked
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C562782 |
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x-linked hypoparathyroidism
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C562782 |
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familial hypocalcemia
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C562783 |
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juvenile myofibromatosis
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C562978 |
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myofibromatosis, infantile
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C562978 |
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branchiogenic-deafness syndrome
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C563780 |
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aarau disease
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C563781 |
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reticular erythrokeratoderma
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C563781 |
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