MESD

mesoderm development LRP chaperone
OMIM: 607783, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green MESD in Skeletal Dysplasia_Fetal Level 2: Skeletal disorders Version 0.230	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Phenotypes Osteogenesis imperfecta, type XX, MIM# 618644
Green MESD in Mendeliome Version 1.2511	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Phenotypes Osteogenesis imperfecta, type XX, MIM# 618644
Green MESD in Osteogenesis Imperfecta and Osteoporosis Level 2: Skeletal disorders Version 1.3	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Phenotypes Osteogenesis imperfecta, type XX, MIM# 618644
Green MESD in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.309	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Phenotypes Osteogenesis imperfecta, type XX, MIM# 618644
Green MESD in Fetal anomalies Version 1.321	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Other Phenotypes Osteogenesis imperfecta, type XX, OMIM:618644 Osteogenesis imperfecta, type 20, MONDO:0032846
Green MESD in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.117	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes Osteogenesis imperfecta, type XX, MIM# 618644 Tags treatable skeletal
Green MESD in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Phenotypes Osteogenesis imperfecta, type XX, MIM# 618644