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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.
isolated congenital adermatoglyphia
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7619 |
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congenital sucrase-isomaltase deficiency with minimal starch tolerance
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17619 |
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primary, 1 ciliary dyskinesia
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D007619 |
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CSID with minimal starch tolerance
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17619 |
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immigration delay disease
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7619 |
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congenital sucrase-isomaltose malabsorption with minimal starch tolerance
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17619 |
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absence of fingerprints
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7619 |
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congenital sucrose intolerance with minimal starch tolerance
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17619 |
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congenital absence of fingerprints
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7619 |
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primary, 1, with or without situs inversus ciliary dyskinesia
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D007619 |
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fingerprints, absence of
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7619 |
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bronchiectasis, and sinusitis dextrocardia
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D007619 |
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krieble bixler syndrome
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C537619 |
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disaccharide intolerance with minimal starch tolerance
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17619 |
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