CTSF

PanelMode of inheritanceDetails
3 panels
R-numbers: R58
Signed-off version 4.41
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ceroid lipofuscinosis, neuronal, 13, Kufs type, OMIM:615362
R-numbers: R276
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ceroid lipofuscinosis, neuronal, 13, Kufs type OMIM:615362, neuronal ceroid lipofuscinosis 13 MONDO:0014147
R-numbers: R231
Signed-off version 2.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ceroid lipofuscinosis, neuronal, 13, Kufs type OMIM:615362, neuronal ceroid lipofuscinosis 13 MONDO:0014147