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Pulmonary Fibrosis_Interstitial Lung Disease v0.130 ASAH1 Zornitza Stark Phenotypes for gene: ASAH1 were changed from Spinal muscular atrophy with progressive myoclonic epilepsy, MIM# 159950; Farber lipogranulomatosis, MIM# 228000 to Spinal muscular atrophy with progressive myoclonic epilepsy, MIM# 159950; Farber lipogranulomatosis, MIM# 228000
Pulmonary Fibrosis_Interstitial Lung Disease v0.129 ASAH1 Zornitza Stark Marked gene: ASAH1 as ready
Pulmonary Fibrosis_Interstitial Lung Disease v0.129 ASAH1 Zornitza Stark Gene: asah1 has been classified as Red List (Low Evidence).
Pulmonary Fibrosis_Interstitial Lung Disease v0.129 ASAH1 Zornitza Stark Phenotypes for gene: ASAH1 were changed from to Spinal muscular atrophy with progressive myoclonic epilepsy, MIM# 159950; Farber lipogranulomatosis, MIM# 228000
Pulmonary Fibrosis_Interstitial Lung Disease v0.128 ASAH1 Zornitza Stark Publications for gene: ASAH1 were set to
Pulmonary Fibrosis_Interstitial Lung Disease v0.127 ASAH1 Zornitza Stark Classified gene: ASAH1 as Red List (low evidence)
Pulmonary Fibrosis_Interstitial Lung Disease v0.127 ASAH1 Zornitza Stark Gene: asah1 has been classified as Red List (Low Evidence).
Pulmonary Fibrosis_Interstitial Lung Disease v0.126 ASAH1 Zornitza Stark edited their review of gene: ASAH1: Added comment: Respiratory insufficiency due to muscle weakness in Spinal muscular atrophy with progressive myoclonic epilepsy, MIM# 159950, does not fit with panel scope.; Changed rating: RED
Pulmonary Fibrosis_Interstitial Lung Disease v0.0 ASAH1 Zornitza Stark gene: ASAH1 was added
gene: ASAH1 was added to Pulmonary Fibrosis_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ASAH1 was set to Unknown