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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 recessive nonsyndromic deafness 18A
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11192 |
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autosomal dominant nonsyndromic deafness 48
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11920 |
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autosomal dominant nonsyndromic deafness caused by mutation in MYO1A
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11920 |
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autosomal recessive nonsyndromic deafness caused by mutation in USH1C
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11192 |
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autosomal recessive nonsyndromic deafness type 18A
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11192 |
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tufted angioma of the skin
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11927 |
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autosomal dominant nonsyndromic deafness type 48
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11920 |
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tufted hemangioma of the skin
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11927 |
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melanoma of the esophagus
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1192 |
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mucosal melanoma of the esophagus
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1192 |
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split notochord syndrome
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11928 |
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1p36 deletion syndrome
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11929 |
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monosomy 1P36 syndrome
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11929 |
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panic disorder susceptibility locus, chromosome 9Q-Related
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http://purl.obolibrary.org/obo/MONDO_0011924 |
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panic disorder susceptibility locus, chromosome 9Q-related
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11924 |
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