TNFRSF11B

TNF receptor superfamily member 11b
OMIM: 602643, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green TNFRSF11B in Mendeliome Version 1.3512	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes juvenile Paget disease MONDO:0009394 chondrocalcinosis 1 MONDO:0010917
Green TNFRSF11B in Osteogenesis Imperfecta and Osteoporosis Level 2: Skeletal disorders Version 1.8	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes juvenile Paget disease MONDO:0009394 chondrocalcinosis 1 MONDO:0010917
Green TNFRSF11B in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.346	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Victorian Clinical Genetics Services Phenotypes juvenile Paget disease MONDO:0009394 chondrocalcinosis 1 MONDO:0010917
Green TNFRSF11B in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.110	0 reviews	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	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Paget disease
Green TNFRSF11B in Prepair 1000+ Level 2: Screening Version 2.14	1 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 1.140	1 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