Activity

Filter

Cancel
Date Panel Item Activity
72 actions
Severe Paediatric Disorders v0.12 MPO Louise Daugherty reviewed gene: MPO: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 MPO Louise Daugherty Publications for gene MPO were updated from to 30847515
Severe Paediatric Disorders v0.11 MPO Louise Daugherty Mode of inheritance for gene MPO was changed from to BIALLELIC, autosomal or pseudoautosomal
Severe Paediatric Disorders v0.10 VCP Louise Daugherty Added phenotypes Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia, 613954; Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1, 167320; Charcot-Marie-Tooth disease, type 2Y, 616687 for gene: VCP
Severe Paediatric Disorders v0.10 TBK1 Louise Daugherty Added phenotypes Frontotemporal dementia and/or amyotrophic lateral sclerosis 4, 616439 for gene: TBK1
Severe Paediatric Disorders v0.10 TARDBP Louise Daugherty Added phenotypes Amyotrophic lateral sclerosis 10, with or without FTD, 612069; Frontotemporal lobar degeneration, TARDBP-related, 612069 for gene: TARDBP
Severe Paediatric Disorders v0.10 SQSTM1 Louise Daugherty Added phenotypes Paget disease of bone 3, 167250; Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset, 617145; Myopathy, distal, with rimmed vacuoles, 617158; Frontotemporal dementia and/or amyotrophic lateral sclerosis 3, 616437 for gene: SQSTM1
Severe Paediatric Disorders v0.10 SOX9 Louise Daugherty Added phenotypes Acampomelic campomelic dysplasia, 114290; Campomelic dysplasia, 114290; Campomelic dysplasia with autosomal sex reversal, 114290 for gene: SOX9
Severe Paediatric Disorders v0.10 SERPING1 Louise Daugherty Added phenotypes Complement component 4, partial deficiency of, 120790; Angioedema, hereditary, types I and II, 106100 for gene: SERPING1
Severe Paediatric Disorders v0.10 PSEN1 Louise Daugherty Added phenotypes ?Acne inversa, familial, 3, 613737; Alzheimer disease, type 3, 607822; Pick disease, 172700; Cardiomyopathy, dilated, 1U, 613694; Dementia, frontotemporal, 600274; Alzheimer disease, type 3, with spastic paraparesis and apraxia, 607822; Alzheimer disease, type 3, with spastic paraparesis and unusual plaques, 607822 for gene: PSEN1
Severe Paediatric Disorders v0.10 MPO Louise Daugherty Added phenotypes Myeloperoxidase deficiency, 254600 for gene: MPO
Severe Paediatric Disorders v0.10 MAPT Louise Daugherty Added phenotypes Pick disease, 172700; Supranuclear palsy, progressive, 601104; Supranuclear palsy, progressive atypical, 260540; Dementia, frontotemporal, with or without parkinsonism, 600274 for gene: MAPT
Severe Paediatric Disorders v0.10 LGI1 Louise Daugherty Added phenotypes Epilepsy, familial temporal lobe, 1, 600512 for gene: LGI1
Severe Paediatric Disorders v0.10 GRN Louise Daugherty Added phenotypes Aphasia, primary progressive, 607485; Ceroid lipofuscinosis, neuronal, 11, 614706; Frontotemporal lobar degeneration with ubiquitin-positive inclusions, 607485 for gene: GRN
Severe Paediatric Disorders v0.10 FIG4 Louise Daugherty Added phenotypes Charcot-Marie-Tooth disease, type 4J, 611228; Yunis-Varon syndrome, 216340; ?Polymicrogyria, bilateral temporooccipital, 612691; Amyotrophic lateral sclerosis 11, 612577 for gene: FIG4
Severe Paediatric Disorders v0.10 CPA6 Louise Daugherty Added phenotypes Epilepsy, familial temporal lobe, 5, 614417; Febrile seizures, familial, 11, 614418 for gene: CPA6
Severe Paediatric Disorders v0.10 CHCHD10 Louise Daugherty Added phenotypes ?Myopathy, isolated mitochondrial, autosomal dominant, 616209; Spinal muscular atrophy, Jokela type, 615048; Frontotemporal dementia and/or amyotrophic lateral sclerosis 2, 615911 for gene: CHCHD10
Severe Paediatric Disorders v0.10 C9orf72 Louise Daugherty Added phenotypes Frontotemporal dementia and/or amyotrophic lateral sclerosis 1, 105550 for gene: C9orf72
Severe Paediatric Disorders v0.9 VCP Louise Daugherty Added phenotypes Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia, 613954; Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1, 167320; Charcot-Marie-Tooth disease, type 2Y, 616687 for gene: VCP
Severe Paediatric Disorders v0.9 TBK1 Louise Daugherty Added phenotypes Frontotemporal dementia and/or amyotrophic lateral sclerosis 4, 616439 for gene: TBK1
Severe Paediatric Disorders v0.9 TARDBP Louise Daugherty Added phenotypes Amyotrophic lateral sclerosis 10, with or without FTD, 612069; Frontotemporal lobar degeneration, TARDBP-related, 612069 for gene: TARDBP
Severe Paediatric Disorders v0.9 SQSTM1 Louise Daugherty Added phenotypes Paget disease of bone 3, 167250; Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset, 617145; Myopathy, distal, with rimmed vacuoles, 617158; Frontotemporal dementia and/or amyotrophic lateral sclerosis 3, 616437 for gene: SQSTM1
Severe Paediatric Disorders v0.9 SOX9 Louise Daugherty Added phenotypes Acampomelic campomelic dysplasia, 114290; Campomelic dysplasia, 114290; Campomelic dysplasia with autosomal sex reversal, 114290 for gene: SOX9
Severe Paediatric Disorders v0.9 SERPING1 Louise Daugherty Added phenotypes Complement component 4, partial deficiency of, 120790; Angioedema, hereditary, types I and II, 106100 for gene: SERPING1
Severe Paediatric Disorders v0.9 PSEN1 Louise Daugherty Added phenotypes ?Acne inversa, familial, 3, 613737; Alzheimer disease, type 3, 607822; Pick disease, 172700; Cardiomyopathy, dilated, 1U, 613694; Dementia, frontotemporal, 600274; Alzheimer disease, type 3, with spastic paraparesis and apraxia, 607822; Alzheimer disease, type 3, with spastic paraparesis and unusual plaques, 607822 for gene: PSEN1
Severe Paediatric Disorders v0.9 MPO Louise Daugherty Added phenotypes Myeloperoxidase deficiency, 254600 for gene: MPO
Severe Paediatric Disorders v0.9 MAPT Louise Daugherty Added phenotypes Pick disease, 172700; Supranuclear palsy, progressive, 601104; Supranuclear palsy, progressive atypical, 260540; Dementia, frontotemporal, with or without parkinsonism, 600274 for gene: MAPT
Severe Paediatric Disorders v0.9 LGI1 Louise Daugherty Added phenotypes Epilepsy, familial temporal lobe, 1, 600512 for gene: LGI1
Severe Paediatric Disorders v0.9 GRN Louise Daugherty Added phenotypes Aphasia, primary progressive, 607485; Ceroid lipofuscinosis, neuronal, 11, 614706; Frontotemporal lobar degeneration with ubiquitin-positive inclusions, 607485 for gene: GRN
Severe Paediatric Disorders v0.9 FIG4 Louise Daugherty Added phenotypes Charcot-Marie-Tooth disease, type 4J, 611228; Yunis-Varon syndrome, 216340; ?Polymicrogyria, bilateral temporooccipital, 612691; Amyotrophic lateral sclerosis 11, 612577 for gene: FIG4
Severe Paediatric Disorders v0.9 CPA6 Louise Daugherty Added phenotypes Epilepsy, familial temporal lobe, 5, 614417; Febrile seizures, familial, 11, 614418 for gene: CPA6
Severe Paediatric Disorders v0.9 CHCHD10 Louise Daugherty Added phenotypes ?Myopathy, isolated mitochondrial, autosomal dominant, 616209; Spinal muscular atrophy, Jokela type, 615048; Frontotemporal dementia and/or amyotrophic lateral sclerosis 2, 615911 for gene: CHCHD10
Severe Paediatric Disorders v0.9 C9orf72 Louise Daugherty Added phenotypes Frontotemporal dementia and/or amyotrophic lateral sclerosis 1, 105550 for gene: C9orf72
Severe Paediatric Disorders v0.9 VCP Louise Daugherty Added phenotypes Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia, 613954; Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1, 167320; Charcot-Marie-Tooth disease, type 2Y, 616687 for gene: VCP
Severe Paediatric Disorders v0.9 TBK1 Louise Daugherty Added phenotypes Frontotemporal dementia and/or amyotrophic lateral sclerosis 4, 616439 for gene: TBK1
Severe Paediatric Disorders v0.9 TARDBP Louise Daugherty Added phenotypes Amyotrophic lateral sclerosis 10, with or without FTD, 612069; Frontotemporal lobar degeneration, TARDBP-related, 612069 for gene: TARDBP
Severe Paediatric Disorders v0.9 SQSTM1 Louise Daugherty Added phenotypes Paget disease of bone 3, 167250; Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset, 617145; Myopathy, distal, with rimmed vacuoles, 617158; Frontotemporal dementia and/or amyotrophic lateral sclerosis 3, 616437 for gene: SQSTM1
Severe Paediatric Disorders v0.9 SOX9 Louise Daugherty Added phenotypes Acampomelic campomelic dysplasia, 114290; Campomelic dysplasia, 114290; Campomelic dysplasia with autosomal sex reversal, 114290 for gene: SOX9
Severe Paediatric Disorders v0.9 SERPING1 Louise Daugherty Added phenotypes Complement component 4, partial deficiency of, 120790; Angioedema, hereditary, types I and II, 106100 for gene: SERPING1
Severe Paediatric Disorders v0.9 PSEN1 Louise Daugherty Added phenotypes ?Acne inversa, familial, 3, 613737; Alzheimer disease, type 3, 607822; Pick disease, 172700; Cardiomyopathy, dilated, 1U, 613694; Dementia, frontotemporal, 600274; Alzheimer disease, type 3, with spastic paraparesis and apraxia, 607822; Alzheimer disease, type 3, with spastic paraparesis and unusual plaques, 607822 for gene: PSEN1
Severe Paediatric Disorders v0.9 MPO Louise Daugherty Added phenotypes Myeloperoxidase deficiency, 254600 for gene: MPO
Severe Paediatric Disorders v0.9 MAPT Louise Daugherty Added phenotypes Pick disease, 172700; Supranuclear palsy, progressive, 601104; Supranuclear palsy, progressive atypical, 260540; Dementia, frontotemporal, with or without parkinsonism, 600274 for gene: MAPT
Severe Paediatric Disorders v0.9 LGI1 Louise Daugherty Added phenotypes Epilepsy, familial temporal lobe, 1, 600512 for gene: LGI1
Severe Paediatric Disorders v0.9 GRN Louise Daugherty Added phenotypes Aphasia, primary progressive, 607485; Ceroid lipofuscinosis, neuronal, 11, 614706; Frontotemporal lobar degeneration with ubiquitin-positive inclusions, 607485 for gene: GRN
Severe Paediatric Disorders v0.9 FIG4 Louise Daugherty Added phenotypes Charcot-Marie-Tooth disease, type 4J, 611228; Yunis-Varon syndrome, 216340; ?Polymicrogyria, bilateral temporooccipital, 612691; Amyotrophic lateral sclerosis 11, 612577 for gene: FIG4
Severe Paediatric Disorders v0.9 CPA6 Louise Daugherty Added phenotypes Epilepsy, familial temporal lobe, 5, 614417; Febrile seizures, familial, 11, 614418 for gene: CPA6
Severe Paediatric Disorders v0.9 CHCHD10 Louise Daugherty Added phenotypes ?Myopathy, isolated mitochondrial, autosomal dominant, 616209; Spinal muscular atrophy, Jokela type, 615048; Frontotemporal dementia and/or amyotrophic lateral sclerosis 2, 615911 for gene: CHCHD10
Severe Paediatric Disorders v0.9 C9orf72 Louise Daugherty Added phenotypes Frontotemporal dementia and/or amyotrophic lateral sclerosis 1, 105550 for gene: C9orf72
Severe Paediatric Disorders v0.8 VCP Louise Daugherty Added phenotypes Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1, 167320; Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia, 613954; Charcot-Marie-Tooth disease, type 2Y, 616687 for gene: VCP
Severe Paediatric Disorders v0.8 TBK1 Louise Daugherty Added phenotypes Frontotemporal dementia and/or amyotrophic lateral sclerosis 4, 616439 for gene: TBK1
Severe Paediatric Disorders v0.8 TARDBP Louise Daugherty Added phenotypes Frontotemporal lobar degeneration, TARDBP-related, 612069; Amyotrophic lateral sclerosis 10, with or without FTD, 612069 for gene: TARDBP
Severe Paediatric Disorders v0.8 SQSTM1 Louise Daugherty Added phenotypes Myopathy, distal, with rimmed vacuoles, 617158; Paget disease of bone 3, 167250; Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset, 617145; Frontotemporal dementia and/or amyotrophic lateral sclerosis 3, 616437 for gene: SQSTM1
Severe Paediatric Disorders v0.8 SOX9 Louise Daugherty Added phenotypes Acampomelic campomelic dysplasia, 114290; Campomelic dysplasia, 114290; Campomelic dysplasia with autosomal sex reversal, 114290 for gene: SOX9
Severe Paediatric Disorders v0.8 SERPING1 Louise Daugherty Added phenotypes Angioedema, hereditary, types I and II, 106100; Complement component 4, partial deficiency of, 120790 for gene: SERPING1
Severe Paediatric Disorders v0.8 PSEN1 Louise Daugherty Added phenotypes Cardiomyopathy, dilated, 1U, 613694; Alzheimer disease, type 3, with spastic paraparesis and unusual plaques, 607822; Dementia, frontotemporal, 600274; Alzheimer disease, type 3, with spastic paraparesis and apraxia, 607822; ?Acne inversa, familial, 3, 613737; Pick disease, 172700; Alzheimer disease, type 3, 607822 for gene: PSEN1
Severe Paediatric Disorders v0.8 MPO Louise Daugherty Added phenotypes Myeloperoxidase deficiency, 254600 for gene: MPO
Severe Paediatric Disorders v0.8 MAPT Louise Daugherty Added phenotypes Dementia, frontotemporal, with or without parkinsonism, 600274; Supranuclear palsy, progressive atypical, 260540; Supranuclear palsy, progressive, 601104; Pick disease, 172700 for gene: MAPT
Severe Paediatric Disorders v0.8 LGI1 Louise Daugherty Added phenotypes Epilepsy, familial temporal lobe, 1, 600512 for gene: LGI1
Severe Paediatric Disorders v0.8 GRN Louise Daugherty Added phenotypes Frontotemporal lobar degeneration with ubiquitin-positive inclusions, 607485; Aphasia, primary progressive, 607485; Ceroid lipofuscinosis, neuronal, 11, 614706 for gene: GRN
Severe Paediatric Disorders v0.8 FIG4 Louise Daugherty Added phenotypes ?Polymicrogyria, bilateral temporooccipital, 612691; Yunis-Varon syndrome, 216340; Charcot-Marie-Tooth disease, type 4J, 611228; Amyotrophic lateral sclerosis 11, 612577 for gene: FIG4
Severe Paediatric Disorders v0.8 CPA6 Louise Daugherty Added phenotypes Febrile seizures, familial, 11, 614418; Epilepsy, familial temporal lobe, 5, 614417 for gene: CPA6
Severe Paediatric Disorders v0.8 CHCHD10 Louise Daugherty Added phenotypes ?Myopathy, isolated mitochondrial, autosomal dominant, 616209; Spinal muscular atrophy, Jokela type, 615048; Frontotemporal dementia and/or amyotrophic lateral sclerosis 2, 615911 for gene: CHCHD10
Severe Paediatric Disorders v0.8 C9orf72 Louise Daugherty Added phenotypes Frontotemporal dementia and/or amyotrophic lateral sclerosis 1, 105550 for gene: C9orf72
Severe Paediatric Disorders v0.8 VCP Louise Daugherty Mode of inheritance for gene VCP was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia, 613954; Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1, 167320; Charcot-Marie-Tooth disease, type 2Y, 616687 for gene: VCP
Severe Paediatric Disorders v0.8 TBK1 Louise Daugherty Mode of inheritance for gene TBK1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Frontotemporal dementia and/or amyotrophic lateral sclerosis 4, 616439 for gene: TBK1
Severe Paediatric Disorders v0.8 TARDBP Louise Daugherty Mode of inheritance for gene TARDBP was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Amyotrophic lateral sclerosis 10, with or without FTD, 612069; Frontotemporal lobar degeneration, TARDBP-related, 612069 for gene: TARDBP
Severe Paediatric Disorders v0.8 SQSTM1 Louise Daugherty Mode of inheritance for gene SQSTM1 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes Paget disease of bone 3, 167250; Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset, 617145; Myopathy, distal, with rimmed vacuoles, 617158; Frontotemporal dementia and/or amyotrophic lateral sclerosis 3, 616437 for gene: SQSTM1
Severe Paediatric Disorders v0.8 SOX9 Louise Daugherty Mode of inheritance for gene SOX9 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Acampomelic campomelic dysplasia, 114290; Campomelic dysplasia, 114290; Campomelic dysplasia with autosomal sex reversal, 114290 for gene: SOX9
Severe Paediatric Disorders v0.8 SERPING1 Louise Daugherty Mode of inheritance for gene SERPING1 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes Complement component 4, partial deficiency of, 120790; Angioedema, hereditary, types I and II, 106100 for gene: SERPING1
Severe Paediatric Disorders v0.7 MPO Louise Daugherty Source Next Generation Children Project was added to MPO.
Severe Paediatric Disorders v0.5 MPO Louise Daugherty Source Expert Review Green was added to MPO.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 MPO Louise Daugherty gene: MPO was added
gene: MPO was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: MPO was set to