Level 3: Motor Disorders of the CNS
Level 2: Neurology and neurodevelopmental disorders
Version 1.9
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review
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BIALLELIC, autosomal or pseudoautosomal
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Sources
- Expert Review Green
- Literature
Phenotypes
- Brain Dopamine Serotonin Vesicular Transport Disease (Other disorders of neurotransmitter metabolism)
- Vesicular monoamine transporter deficiency
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Level 3: Specific metabolic abnormalities
Level 2: Metabolic disorders
Version 1.617
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review
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BIALLELIC, autosomal or pseudoautosomal
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Sources
- Expert Review Green
- Literature
Phenotypes
- Brain Dopamine Serotonin Vesicular Transport Disease (Other disorders of neurotransmitter metabolism)
- Brain Dopamine Serotonin Vesicular Transport Disease (Other disorders of neurotransmitter metabolism) (NO phenotype number in OMIM)
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Version 5.3
Latest signed off version: v5.0
(1 May 2024)
Component of the following Super Panels:
Childhood onset leukodystrophy
Hypotonic infant
Paediatric disorders
Unexplained death in infancy and sudden unexplained death in childhood
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review
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BIALLELIC, autosomal or pseudoautosomal
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Sources
- Expert Review Green
- London North GLH
- NHS GMS
Phenotypes
- Brain Dopamine Serotonin Vesicular Transport Disease (Other disorders of neurotransmitter metabolism)
- Brain Dopamine Serotonin Vesicular Transport Disease (Other disorders of neurotransmitter metabolism) (NO phenotype number in OMIM)
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Version 4.3
Latest signed off version: v4.0
(1 May 2024)
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review
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BIALLELIC, autosomal or pseudoautosomal
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Sources
- NHS GMS
- Expert Review Green
- PanelApp
- London North GLH
Phenotypes
- ?Parkinsonism-dystonia, infantile, 2, OMIM:618049
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Version 1.184
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review
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BIALLELIC, autosomal or pseudoautosomal
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Sources
- Next Generation Children Project
- Expert Review Amber
- Expert list
Phenotypes
- ?Spinal muscular atrophy, distal, autosomal recessive, 2, 605726
- ?Amyotrophic lateral sclerosis 16, juvenile, 614373
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