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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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dyserythropoietic Anemia, congenital, type 2
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9134 |
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severe combined immunodeficiency due to CARMIL2 deficiency
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29134 |
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dyserythropoietic Anemia, hempas type
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9134 |
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motor neuronopathies, hereditary
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D009134 |
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motor neuronopathy, hereditary
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D009134 |
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neuronopathy, hereditary motor
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D009134 |
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muscular atrophy, spinal
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D009134 |
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scapuloperoneal form of spinal muscular atrophy
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D009134 |
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muscular atrophies, progressive
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D009134 |
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muscular atrophy, progressive
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D009134 |
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muscular atrophy, myelopathic
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D009134 |
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progressive proximal myelopathic muscular atrophy
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D009134 |
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hereditary motor neuronopathies
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D009134 |
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hereditary motor neuronopathy
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D009134 |
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neurogenic scapuloperoneal, new england type amyotrophy
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D009134 |
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