MEOX1

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green MEOX1 in Skeletal Dysplasia_Fetal Level 2: Skeletal disorders Version 0.225	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Klippel-Feil syndrome 2, OMIM:214300 Klippel-Feil syndrome 2, autosomal recessive, MONDO:0008958
Green MEOX1 in Mendeliome Version 1.2302	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Klippel-Feil syndrome 2, OMIM:214300 Klippel-Feil syndrome 2, autosomal recessive, MONDO:0008958
Green MEOX1 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.302	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Green Expert list Radboud University Medical Center, Nijmegen NHS GMS Victorian Clinical Genetics Services Phenotypes Klippel-Feil syndrome 2 214300
Amber MEOX1 in Clefting disorders Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 0.260	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Phenotypes KLIPPEL-FEIL SYNDROME 2, AUTOSOMAL RECESSIVE KFS2
Green MEOX1 in Fetal anomalies Version 1.313	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Klippel-Feil syndrome 2, OMIM:214300 Klippel-Feil syndrome 2, autosomal recessive, MONDO:0008958

5 panels