MEIS2

Meis homeobox 2
OMIM: 601740, ClinGen, DECIPHER

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green MEIS2 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.430	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cleft palate, cardiac defects, and mental retardation (MIM#600987)
Green MEIS2 in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cleft palate, cardiac defects, and mental retardation (MIM#600987)
Green MEIS2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genetic Health Queensland Phenotypes Cleft palate, cardiac defects, and mental retardation (MIM#600987)
Green MEIS2 in Clefting disorders Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 0.260	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Victorian Clinical Genetics Services Expert Review Green Phenotypes intellectual disability cardiac defects Orofacial clefting Cleft palate
Green MEIS2 in Fetal anomalies Version 1.313	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Phenotypes Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies, MONDO:0010970 Cleft palate, cardiac defects, and mental retardation, OMIM:600987
Amber MEIS2 in Speech apraxia Level 2: Neurology and neurodevelopmental disorders Version 1.27	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert list Expert Review Phenotypes Cleft palate, cardiac defects, and impaired intellectual development, MIM# 600987