autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation
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14711 |
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autosomal dominant Charcot-Marie-Tooth disease type 2W
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14711 |
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2W
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14711 |
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Charcot-Marie-Tooth disease, axonal type 2W
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14711 |
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Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2W
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14711 |
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Charcot-Marie-Tooth disease, axonal, type 2W
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14711 |
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Charcot-Marie-Tooth disease, axonal, type 2W; CMT2W
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http://purl.obolibrary.org/obo/MONDO_0014711 |
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Charcot-Marie-Tooth disease, axonal, type 2w
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14711 |
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HARS Charcot-Marie-Tooth disease type 2
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14711 |
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Charcot-Marie-Tooth disease type 2 caused by mutation in HARS
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14711 |
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Charcot-Marie-Tooth neuropathy type 2W
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14711 |
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Charcot-Marie-Tooth neuropathy, type 2W
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14711 |
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