Panel | Mode of inheritance | Details |
---|---|---|
6 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes MUCOPOLYSACCHARIDOSIS TYPE 4A 253000 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes MUCOPOLYSACCHARIDOSIS TYPE 4A |
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 4A, Mucopolysaccharidosis Type IVA, Mucopolysaccharidosis IVA, 253000, Mucopolysaccharidosis, Type IV, MPS IVA, Morquio A disease (MPS IV, Morquio disease) |
Green in Lysosomal storage disorderR-numbers: R276 Signed-off version 3.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Mucopolysaccharidosis IVA OMIM:253000, mucopolysaccharidosis type 4A MONDO:0009659 |
Green in Mucopolysaccharidosis type IVAR-numbers: R287 Signed-off version 1.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes |
Green in Skeletal dysplasiaComponent of the following Super Panels:
R-numbers: R104 Signed-off version 5.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Mucopolysaccharidosis IVA 253000 |