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| license |
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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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autosomal dominant (PSN) peripheral sensory neuropathy
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C537989 |
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distal deletion 14q
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19898 |
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distal monosomy 14q
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19898 |
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telomeric deletion 14q
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19898 |
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distal deletion 19p
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19893 |
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telomeric deletion 19p
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19893 |
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distal monosomy 19p13.3
|
19893 |
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MRKH, type 2
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10989 |
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fibroxanthoma NOS (morphologic abnormality)
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2989 |
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deficiencies, alpha 1-antitrypsin
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D019896 |
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deficiency, alpha 1-antitrypsin
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D019896 |
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distal deletion 7p
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19892 |
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distal deletion 12q
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19897 |
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distal monosomy 12q
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19897 |
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cutaneous leishmaniasis (subtype)
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11989 |
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