Panel | Mode of inheritance | Details |
---|---|---|
4 panels | ||
R-numbers: R56 Signed-off version 4.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Basal ganglia calcification, idiopathic, 5, OMIM:615483 |
R-numbers: R58 Signed-off version 6.6 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Basal ganglia calcification, idiopathic, 5, OMIM:615483 |
R-numbers: R57 Signed-off version 5.4 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Basal ganglia calcification, idiopathic, 5, OMIM:615483, basal ganglia calcification, idiopathic, 5, MONDO:0014204 |
Component of the following Super Panels:
Signed-off version 5.3 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Fahr syndrome, Basal ganglia calcification, idiopathic, 5, 615483 |