Panel | Mode of inheritance | Details |
---|---|---|
3 panels | ||
Component of the following Super Panels:
Signed-off version 4.40 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Spastic paraplegia 79B, autosomal recessive, OMIM:615491, early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome, MONDO:0014209, Spastic paraplegia 79A, autosomal dominant, OMIM:620221 |
R-numbers: R61 Signed-off version 4.28 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Spastic paraplegia 79B, autosomal recessive, OMIM:615491, early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome, MONDO:0014209, Spastic paraplegia 79A, autosomal dominant, OMIM:620221 |
Green in Optic neuropathyR-numbers: R41 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Spastic paraplegia 79, autosomal recessive, 615491 |