Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.15 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes NEUROPATHY, CONGENITAL HYPOMYELINATING, 1 605253 |
R-numbers: R78 Signed-off version 5.16 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Charcot-Marie-Tooth, Type 1, Charcot Marie Tooth disease, type 1D, 607678 |