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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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total premature chromatid separation trait
|
8304 |
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childhood mesenchymal chondrosarcoma
|
3041 |
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ring 18 chromosome syndrome
|
C538304 |
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autosomal recessive complex spastic paraplegia caused by mutation in ARL6IP1
|
14304 |
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thymic large cell neuroendocrine carcinoma
|
3047 |
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thymus large cell neuroendocrine carcinoma
|
3047 |
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ovarian large cell neuroendocrine carcinoma
|
3049 |
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ovary large cell neuroendocrine carcinoma
|
3049 |
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parathyroid mixed cell type adenoma
|
4304 |
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auditory disease, central
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D001304 |
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auditory diseases, central
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D001304 |
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auditory dysfunction, central
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D001304 |
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pediatric mesenchymal chondrosarcoma
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3041 |
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adult mesenchymal chondrosarcoma
|
3042 |
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obsolete extraosseous chondrosarcoma
|
3044.0 |
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