C15orf41:Ensemblv90

chromosome 15 open reading frame 41
OMIM: 615626, ClinGen, DECIPHER

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green C15orf41 in Bone Marrow Failure Level 2: Haematological disorders Version 1.131 Component of the following Super Panels: Immunological disorders_SuperPanel	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Dyserythropoietic anemia, congenital, type Ib, MIM# 615631
Green C15orf41 in Mendeliome Version 1.3802	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Dyserythropoietic anemia, congenital, type Ib, MIM# 615631
Green C15orf41 in Red cell disorders Level 2: Haematological disorders Version 1.39	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Yorkshire and North East GLH NHS GMS Wessex and West Midlands GLH North West GLH London South GLH Phenotypes Dyserythropoietic anaemia, congenital, type Ib, MIM# 615631
Green C15orf41 in IBMDx study Version 0.38	1 review	Unknown	Sources Expert Review Green IBMDx Study Expert Review Green Expert list Phenotypes Dyserythropoietic anemia, congenital, type Ib, MIM# 615631
Green C15orf41 in Bone Marrow Failure Level 2: Haematological disorders Version 2.0	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Green Phenotypes Dyserythropoietic anemia, congenital, type Ib, MIM# 615631
Green C15orf41 in Red cell disorders Level 2: Haematological disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources London South GLH North West GLH Wessex and West Midlands GLH NHS GMS Yorkshire and North East GLH Expert list Expert Review Green Phenotypes Dyserythropoietic anaemia, congenital, type Ib, MIM# 615631
Green C15orf41 in IBMDx study Version 1.0	1 review	Unknown	Sources Expert list Expert Review Green IBMDx Study Expert Review Green Phenotypes Dyserythropoietic anemia, congenital, type Ib, MIM# 615631