Panel | Mode of inheritance | Details |
---|---|---|
9 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes MUCOPOLYSACCHARIDOSIS TYPE 6 253200 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes MUCOPOLYSACCHARIDOSIS TYPE 6 |
Green in HydrocephalusR-numbers: R86 Signed-off version 4.6 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Mucopolysaccharidosis type VI (Maroteaux-Lamy), OMIM:253200 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 6.13 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes MUCOPOLYSACCHARIDOSIS TYPE 6 (MPS6) |
Green in Likely inborn error of metabolismComponent of the following Super Panels:
R-numbers: R98 Signed-off version 5.6 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes MUCOPOLYSACCHARIDOSIS TYPE 6, Mucopolysaccharidosis, Type VI, Mucopolysaccharidosis type VI (Maroteaux-Lamy), 253200, Mucopolysaccharidosis Type VI, MPS VI, Maroteaux - Lamy disease (MPS IV, Morquio disease) |
Green in Lysosomal storage disorderR-numbers: R276 Signed-off version 3.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Mucopolysaccharidosis type VI (Maroteaux-Lamy) OMIM:253200, mucopolysaccharidosis type 6 MONDO:0009661 |
Green in Mucopolysaccharidosis type VIR-numbers: R290 Signed-off version 1.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes |
R-numbers: R100 Signed-off version 5.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Mucopolysaccharidosis VI (MPS6) 253200 |
Green in Skeletal dysplasiaComponent of the following Super Panels:
R-numbers: R104 Signed-off version 5.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Mucopolysaccharidosis type VI (Maroteaux-Lamy) 253200, Mucopolysaccharidosis type VI (Maroteaux-Lamy) 253200 |