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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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IBMPFD2
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14178 |
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HNRNPA2B1 inclusion body myopathy with Paget disease of bone and frontotemporal dementia
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14178 |
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chromosomal translocation
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D014178 |
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chromosomal translocations
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D014178 |
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genetic translocation
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D014178 |
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genetic translocations
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D014178 |
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translocation, chromosomal
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D014178 |
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translocation, genetic
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D014178 |
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translocations, chromosomal
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D014178 |
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translocations, genetic
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D014178 |
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multisystem Proteinopathy 2
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14178 |
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inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA2B1
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14178 |
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inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2
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14178 |
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inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2; IBMPFD2
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http://purl.obolibrary.org/obo/MONDO_0014178 |
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inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 2
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14178 |
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