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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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BDMR
|
10886 |
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Del(2)(q37)
|
10886 |
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deletion 2q37
|
10886 |
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deletion 2q37-qter
|
10886 |
|
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monosomy 2q37-qter
|
10886 |
|
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Albright hereditary osteodystrophy type 3
|
10886 |
|
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brachydactyly intellectual disability syndrome
|
10886 |
|
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chromosome 2q37 deletion syndrome
|
10886 |
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Albright hereditary osteodystrophy-like syndrome
|
10886 |
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brachydactyly mental retardation syndrome
|
10886 |
|
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2q37 deletion syndrome
|
10886 |
|
|
2q37 microdeletion syndrome
|
10886 |
|
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brachydactyly-intellectual disability syndrome
|
10886 |
|
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brachydactyly-mental retardation syndrome
|
10886 |
|
