Activity
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Arthrogryposis v3.123
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CHRND
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Ivone Leong Phenotypes for gene: CHRND were changed from Myasthenic syndrome, congenital, 3A, slow-channel 616321; ?Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency 616323; Multiple pterygium syndrome, lethal type 253290; Myasthenic syndrome, congenital, 3B, fast-channel 616322 to Multiple pterygium syndrome, lethal type, OMIM:253290
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Arthrogryposis
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CHRND
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Alice Gardham marked CHRND as ready
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Arthrogryposis
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CHRND
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Alice Gardham reviewed CHRND
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