Panel | Mode of inheritance | Details |
---|---|---|
3 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 3.79 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, OMIM:613640 |
R-numbers: R78 Signed-off version 3.66 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Hereditary Sensory and Autonomic Neuropathy, Type IC, Neuropathy, hereditary sensory and autonomic, type IC, 613640 |
Component of the following Super Panels:
R-numbers: R98 Signed-off version 4.78 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Charcot-Marie-Tooth disease, Serine palmitoyl transferase deficiency (Disorders of complex lipid synthesis), Familial dysautonomia |