| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Hereditary Spastic Paraplegia - adult onset v0.59 | CAPN1 | Zornitza Stark Marked gene: CAPN1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia - adult onset v0.59 | CAPN1 | Zornitza Stark Gene: capn1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia - adult onset v0.59 | CAPN1 | Zornitza Stark Phenotypes for gene: CAPN1 were changed from Spastic paraplegia 76 autosomal recessive, 616907 to Spastic paraplegia 76 autosomal recessive, 616907; MONDO:0014827 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia - adult onset v0.58 | CAPN1 | Zornitza Stark Publications for gene: CAPN1 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia - adult onset v0.23 | CAPN1 |
Zornitza Stark changed review comment from: 8 individuals from three families reported. Sources: Expert list; to: 8 individuals from three families reported, predominantly young adult onset. Sources: Expert list |
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| Hereditary Spastic Paraplegia - adult onset v0.0 | CAPN1 |
Bryony Thompson gene: CAPN1 was added gene: CAPN1 was added to Hereditary Spastic Paraplegia - adult onset_RMH. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: CAPN1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CAPN1 were set to Spastic paraplegia 76 autosomal recessive, 616907 |
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