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Severe Paediatric Disorders v0.17 HINT1 Louise Daugherty Mode of inheritance for gene HINT1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Severe Paediatric Disorders v0.12 HINT1 Louise Daugherty reviewed gene: HINT1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 HINT1 Louise Daugherty Publications for gene HINT1 were updated from to 30847515
Severe Paediatric Disorders v0.10 HINT1 Louise Daugherty Added phenotypes Neuromyotonia and axonal neuropathy, autosomal recessive, 137200 for gene: HINT1
Severe Paediatric Disorders v0.9 HINT1 Louise Daugherty Added phenotypes Neuromyotonia and axonal neuropathy, autosomal recessive, 137200 for gene: HINT1
Severe Paediatric Disorders v0.9 HINT1 Louise Daugherty Added phenotypes Neuromyotonia and axonal neuropathy, autosomal recessive, 137200 for gene: HINT1
Severe Paediatric Disorders v0.8 HINT1 Louise Daugherty Added phenotypes Neuromyotonia and axonal neuropathy, autosomal recessive, 137200 for gene: HINT1
Severe Paediatric Disorders v0.7 HINT1 Louise Daugherty Source Next Generation Children Project was added to HINT1.
Severe Paediatric Disorders v0.5 HINT1 Louise Daugherty Source Expert Review Green was added to HINT1.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 HINT1 Louise Daugherty gene: HINT1 was added
gene: HINT1 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: HINT1 was set to