HPGD

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green HPGD in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hypertrophic osteoarthropathy, primary, autosomal recessive 1 MIM#259100 Cranioosteoarthropathy MIM#259100
Green HPGD in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.285	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Phenotypes Digital clubbing, isolated congenital 119900 Cranioosteoarthropathy 259100 Hypertrophic osteoarthropathy, primary, autosomal recessive 1 259100
Green HPGD 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 Cranioosteoarthropathy, 259100 (3)
Red HPGD in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Genomics England PanelApp Phenotypes Hypertrophic osteoarthropathy, primary, autosomal recessive 1 MIM#259100 Cranioosteoarthropathy MIM#259100
Green HPGD in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Cranioosteoarthropathy, 259100 (3)

5 panels