MSX1

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green MSX1 in Mendeliome Version 1.3512	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Witkop syndrome (Ectodermal Dysplasia) (MIM: 189500),Cleft Lip+/- Cleft Palate (Rofacial Cleft- MIM :608874), Oligodontia
Green MSX1 in Oligodontia Level 2: Dysmorphic and congenital abnormality syndromes Version 0.30	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green MSX1 in Ectodermal Dysplasia Level 2: Dermatological disorders Version 0.102	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Ectodermal dysplasia 3, Witkop type, 189500
Green MSX1 in Clefting disorders Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Radboud University Medical Center, Nijmegen Expert Review Green Phenotypes Tooth agenesis, selective, 1, with or without orofacial cleft, 106600 Orofacial cleft 5, 608874 Cleft lip CLP with dental anomalies
Green MSX1 in Fetal anomalies Version 1.465	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Phenotypes Orofacial cleft 5 (MIM#608874)

5 panels