PRDM5

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green PRDM5 in Aortopathy_Connective Tissue Disorders Level 2: Cardiovascular disorders Version 1.86	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Brittle cornea syndrome 2, MIM#614170
Green PRDM5 in Corneal Dystrophy Level 2: Ophthalmological disorders Version 1.11	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Brittle cornea syndrome 2, MIM# 614170
Green PRDM5 in Mendeliome Version 1.2302	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Brittle cornea syndrome 2, MIM# 614170
Green PRDM5 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Brittle cornea syndrome 2, 614170 (3)
Green PRDM5 in Prepair 1000+ Level 2: Screening Version 1.1566	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Brittle cornea syndrome 2, MIM#614170
Green PRDM5 in Prepair 500+ Level 2: Screening Version 1.5	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Brittle cornea syndrome 2, 614170 (3)

6 panels