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Dystonia, chorea or related movement disorder, childhood onset v4.3 L2HGDH Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: L2HGDH.
Dystonia, chorea or related movement disorder, childhood onset v4.3 L2HGDH Achchuthan Shanmugasundram commented on gene: L2HGDH: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Dystonia, chorea or related movement disorder, childhood onset v4.2 L2HGDH Achchuthan Shanmugasundram Source Expert Review Green was added to L2HGDH.
Source NHS GMS was added to L2HGDH.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Dystonia, chorea or related movement disorder, childhood onset v3.38 L2HGDH Achchuthan Shanmugasundram changed review comment from: PMID:15824270 - A 15 year-old boy with L-2-hydroxyglutaric aciduria was reported with early infantile-onset progressive psychomotor regression, mild choreodystonia affecting the distal part of the upper limbs, pyramidal signs, and epilepsy.

PMID:18780161 - Of seven patients from three unrelated Tunisian families with L-2-hydroxyglutaric aciduria and with homozygous variants in L2HGDH gene, three patients from two different families had dystonia.

PMID:24753671 - Two siblings were reported with dystonia diagnosed by classical neuroimaging findings with elevated urinary 2 hydroxyglutaric acid.; to: PMID:15824270 - A 15 year-old boy with L-2-hydroxyglutaric aciduria was reported with early infantile-onset progressive psychomotor regression, mild choreodystonia affecting the distal part of the upper limbs, pyramidal signs, and epilepsy.

PMID:18780161 - Of seven patients from three unrelated Tunisian families with L-2-hydroxyglutaric aciduria and with homozygous variants in L2HGDH gene, three patients from two different families had dystonia. The age of onset of the disorder in these patients is around six years.

PMID:24753671 - Two siblings (13 and 16 years of age with disease onset at 10 years of age) were reported with dystonia diagnosed by classical neuroimaging findings with elevated urinary 2 hydroxyglutaric acid.
Dystonia, chorea or related movement disorder, childhood onset v3.27 L2HGDH Achchuthan Shanmugasundram Tag Q3_23_promote_green tag was added to gene: L2HGDH.
Dystonia, chorea or related movement disorder, childhood onset v3.27 L2HGDH Achchuthan Shanmugasundram Classified gene: L2HGDH as Amber List (moderate evidence)
Dystonia, chorea or related movement disorder, childhood onset v3.27 L2HGDH Achchuthan Shanmugasundram Gene: l2hgdh has been classified as Amber List (Moderate Evidence).
Dystonia, chorea or related movement disorder, childhood onset v3.26 L2HGDH Achchuthan Shanmugasundram Mode of inheritance for gene: L2HGDH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Dystonia, chorea or related movement disorder, childhood onset v3.25 L2HGDH Achchuthan Shanmugasundram Phenotypes for gene: L2HGDH were changed from L-2-hydroxyglutaric aciduria, 236792 to L-2-hydroxyglutaric aciduria, OMIM:236792
Dystonia, chorea or related movement disorder, childhood onset v3.24 L2HGDH Achchuthan Shanmugasundram Publications for gene: L2HGDH were set to
Dystonia, chorea or related movement disorder, childhood onset v3.23 L2HGDH Achchuthan Shanmugasundram reviewed gene: L2HGDH: Rating: GREEN; Mode of pathogenicity: None; Publications: 15824270, 18780161, 24753671; Phenotypes: L-2-hydroxyglutaric aciduria, OMIM:236792; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Dystonia, chorea or related movement disorder, childhood onset v1.49 L2HGDH Zornitza Stark reviewed gene: L2HGDH: Rating: GREEN; Mode of pathogenicity: None; Publications: 24753671, 18780161, 15824270, 10399870; Phenotypes: L-2-hydroxyglutaric aciduria MIM#236792; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Dystonia, chorea or related movement disorder, childhood onset v0.258 L2HGDH Louise Daugherty commented on gene: L2HGDH
Dystonia, chorea or related movement disorder, childhood onset v0.14 L2HGDH Ellen McDonagh Classified gene: L2HGDH as Amber List (moderate evidence)
Dystonia, chorea or related movement disorder, childhood onset v0.14 L2HGDH Ellen McDonagh Gene: l2hgdh has been classified as Amber List (Moderate Evidence).
Dystonia, chorea or related movement disorder, childhood onset v0.1 L2HGDH Ellen McDonagh Source South West GLH was added to L2HGDH.
Mode of inheritance for gene L2HGDH was changed from to Unknown
Added phenotypes L-2-hydroxyglutaric aciduria, 236792 for gene: L2HGDH
Dystonia, chorea or related movement disorder, childhood onset v0.0 PHGDH Ellen McDonagh gene: PHGDH was added
gene: PHGDH was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red
Mode of inheritance for gene: PHGDH was set to
Dystonia, chorea or related movement disorder, childhood onset v0.0 L2HGDH Ellen McDonagh gene: L2HGDH was added
gene: L2HGDH was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red
Mode of inheritance for gene: L2HGDH was set to
Dystonia, chorea or related movement disorder, childhood onset v0.0 HGD Ellen McDonagh gene: HGD was added
gene: HGD was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red
Mode of inheritance for gene: HGD was set to
Dystonia, chorea or related movement disorder, childhood onset v0.0 D2HGDH Ellen McDonagh gene: D2HGDH was added
gene: D2HGDH was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red
Mode of inheritance for gene: D2HGDH was set to