HOXA11

homeobox A11
OMIM: 142958, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Amber HOXA11 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.52	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert list Phenotypes Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MM# 605432
Amber HOXA11 in Bone Marrow Failure Level 2: Haematological disorders Version 1.114 Component of the following Super Panels: Immunological disorders_SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MIM# 605432
Amber HOXA11 in Mendeliome Version 1.2374	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MIM# 605432
Red HOXA11 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.305	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert Review Red UKGTN Radboud University Medical Center, Nijmegen NHS GMS Expert list Victorian Clinical Genetics Services Phenotypes Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 605432
Amber HOXA11 in Fetal anomalies Version 1.314	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 , OMIM #605432
Green HOXA11 in IBMDx study Version 0.35	review	Unknown	Sources Expert Review Green IBMDx Study Expert Review Amber Victorian Clinical Genetics Services Phenotypes Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MIM# 605432