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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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congenital muscular dystrophy caused by mutation in LAMA2
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11925 |
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congenital muscular dystrophy due to laminin alpha2 deficiency
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11925 |
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congenital muscular dystrophy type 1A
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11925 |
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melanoma (disease) of esophagus
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1192 |
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hereditary cold fingers
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D011928 |
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autosomal recessive nonsyndromic deafness 18A
|
11192 |
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autosomal dominant nonsyndromic deafness 48
|
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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autosomal dominant nonsyndromic deafness type 48
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11920 |
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merosin-negative congenital muscular dystrophy
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11925 |
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LAMA2 congenital muscular dystrophy
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11925 |
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merosin-deficient congenital muscular dystrophy
|
11925 |
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congenital merosin-deficient muscular dystrophy 1A
|
11925 |
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