TNFRSF11B

TNF receptor superfamily member 11b
OMIM: 602643, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green TNFRSF11B in Mendeliome Version 1.2512	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Paget disease of bone 5, juvenile-onset, MIM# 239000
Green TNFRSF11B in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.309	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Green NHS GMS Victorian Clinical Genetics Services Phenotypes Paget disease of bone 5, juvenile-onset 239000 Paget disease of bone 5, juvenile-onset 239000
Green TNFRSF11B 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 Paget disease of bone 5, juvenile-onset, 239000 (3)
Green TNFRSF11B in Additional findings_Paediatric Level 2: Screening Version 0.278	review	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Paget disease
Green TNFRSF11B in Prepair 1000+ Level 2: Screening Version 2.7	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Paget disease of bone 5, juvenile-onset MIM#239000
Amber TNFRSF11B in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.117	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber BabySeq Category A gene Phenotypes Paget disease of bone 5, juvenile-onset MIM#239000 Tags for review skeletal