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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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Charcot-Marie-Tooth disease, recessive intermediate, B
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13338 |
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MSRB3 autosomal recessive nonsyndromic deafness
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13386 |
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POLR1D Treacher-Collins syndrome
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13385 |
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deafness, autosomal recessive type 74
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13386 |
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vertigo, episodic recurrent
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D020338 |
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vertigos, episodic recurrent
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D020338 |
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vestibular neuritides, recurrent
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D020338 |
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vestibular neuritis, recurrent
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D020338 |
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acquired pure red cell aplasia
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20338 |
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adult pure red cell aplasia
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20338 |
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idiopathic pure red cell aplasia
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20338 |
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adult pure red-cell aplasia
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20338 |
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X-linked distal spinal muscular atrophy type 3
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10338 |
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Brachydactyly-distal symphalangism syndrome
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C537338 |
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vestibular neuritides, subacute
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D020338 |
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