MESD

mesoderm development LRP chaperone
OMIM: 607783
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 2.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Osteogenesis imperfecta, type XX, OMIM:618644, Osteogenesis imperfecta, type 20, MONDO:0032846
R-numbers: R102
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Osteogenesis imperfecta, type XX, OMIM:618644, Osteogenesis imperfecta, type 20, MONDO:0032846
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Osteogenesis imperfecta, type XX, OMIM:618644, Osteogenesis imperfecta, type 20, MONDO:0032846