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Level 3: Motor and Sensory Disorders of the PNS
Level 2: Neurology and neurodevelopmental disorders
Version 1.478
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review
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
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Sources
- NHS GMS
- South West GLH
- Expert Review Red
- Emory Genetics Laboratory
- UKGTN
- Radboud University Medical Center, Nijmegen
- Expert list
Phenotypes
- Charcot Marie Tooth disease, foot deformity of, 192950
- Charcot Marie Tooth disease, foot deformity of, 192950
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Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.13
Latest signed off version: v6.0
(1 May 2024)
Component of the following Super Panels:
Childhood onset leukodystrophy
Hypotonic infant
Paediatric disorders
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review
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Not set
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Sources
- Victorian Clinical Genetics Services
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Version 4.11
Latest signed off version: v4.0
(1 May 2024)
|
review
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
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Sources
- Radboud University Medical Center, Nijmegen
- South West GLH
- Expert Review Red
- UKGTN
- Emory Genetics Laboratory
- Expert list
- NHS GMS
- NHS GMS
- South West GLH
Phenotypes
- Charcot Marie Tooth disease, foot deformity of, 192950
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