ALX4

ALX homeobox 4
OMIM: 605420, Gene2Phenotype

11 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 11 panels
Green ALX4 in Craniosynostosis Level 2: Dysmorphic and congenital abnormality syndromes Version 1.68	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Frontonasal dysplasia 2 MIM#613451 Parietal foramina 2 MIM#609597
Green ALX4 in Frontonasal dysplasia Level 2: Dysmorphic and congenital abnormality syndromes Version 1.1	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Frontonasal dysplasia 2, MIM# 613451
Green ALX4 in Mendeliome Version 1.1902	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Frontonasal dysplasia 2 MIM# 613451 Parietal foramina 2 MIM# 609597 {Craniosynostosis 5, susceptibility to} MIM#615529
Amber ALX4 in Pierre Robin Sequence Level 2: Dysmorphic and congenital abnormality syndromes Version 0.47	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Frontonasal dysplasia 2, MIM# 613451 FND2 with alopecia
Red ALX4 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.33 Component of the following Super Panels: Progressive Neurological Conditions	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Red Expert Review Phenotypes Parietal foramina 2, MIM# 609597
Green ALX4 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.522	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Amber ALX4 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Genetic Health Queensland Phenotypes Frontonasal dysplasia 2, MIM# 613451
Green ALX4 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.285	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Green NHS GMS Phenotypes Frontonasal dysplasia 2 613451
Green ALX4 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Parietal foramina 2
Green ALX4 in Fetal anomalies Version 1.255	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Frontonasal dysplasia 2, MIM# 613451 Parietal foramina 2, MIM# 609597
Red ALX4 in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category A gene Phenotypes {Craniosynostosis 5, susceptibility to} MIM#615529 Parietal foramina 2 MIM# 609597 Frontonasal dysplasia 2 MIM# 613451