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| language |
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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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AI1F
|
14560 |
|
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ANXD1
|
54560 |
|
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PDA
|
24560 |
|
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PDA1
|
24560 |
|
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anauxetic dysplasia
|
54560 |
|
|
x-linked, syndromic 10 mental retardation
|
C564560 |
|
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amelogenesis imperfecta type 1F
|
14560 |
|
|
3-Hydroxyacyl-CoA dehydrogenase II deficiency
|
C564560 |
|
|
Hydroxyacyl-CoA dehydrogenase II deficiency
|
C564560 |
|
|
spondyloepimetaphyseal dysplasia, anauxetic type
|
54560 |
|
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spondylometaepiphyseal dysplasia, anauxetic type
|
54560 |
|
|
amelogenesis imperfecta caused by mutation in AMBN
|
14560 |
|
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tumor of follicular infundibulum
|
4560 |
|
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amelogenesis imperfecta, hypoplastic type 1F
|
14560 |
|
|
amelogenesis imperfecta hypoplastic type IF
|
14560 |
|
