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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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AI3
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7538 |
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AI3A
|
7538 |
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ADHCAI
|
7538 |
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segmentation syndrome 1
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C537538 |
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autosomal dominant amelogenesis imperfecta hypocalcification type
|
7538 |
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bifid halluces, bilateral
|
17538 |
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bifid hallux, bilateral
|
17538 |
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amelogenesis imperfecta caused by mutation in FAM83H
|
7538 |
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amelogenesis imperfecta, hypocalcification type, autosomal dominant
|
7538 |
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amelogenesis imperfecta hypomineralization type
|
7538 |
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amelogenesis imperfecta, hypomineralization type
|
7538 |
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FAM83H amelogenesis imperfecta
|
7538 |
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Preaxial polydactyly of toes, bilateral
|
17538 |
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bifid great toes, bilateral
|
17538 |
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amelogenesis imperfecta type 3
|
7538 |
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