FANCM

Fanconi anemia complementation group M
OMIM: 609644, Gene2Phenotype

12 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 12 panels
Red FANCM in Bone Marrow Failure Level 2: Haematological disorders Version 1.129 Component of the following Super Panels: Immunological disorders_SuperPanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Fanconi anaemia Tags refuted
Red FANCM in Chromosome Breakage Disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 1.24	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Fanconi anaemia Tags refuted
Green FANCM in Mendeliome Version 1.3512	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Spermatogenic failure 28, MIM# 618086 Premature ovarian failure 15 MIM#618096
Red FANCM in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.132	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Fanconi anaemia Tags refuted
Red FANCM in Radial Ray Abnormalities Level 2: Dysmorphic and congenital abnormality syndromes Version 1.19 Component of the following Super Panels: Limb and Digital Malformations SuperPanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Fanconi anaemia Tags refuted
Green FANCM in Primary Ovarian Insufficiency_Premature Ovarian Failure Level 3: Gonadal and sex development disorders Level 2: Endocrine disorders Version 0.388	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health QLD Victorian Clinical Genetics Services Phenotypes Premature ovarian failure 15 MIM#618096
Red FANCM in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category C gene Phenotypes Fanconi anaemia
Red FANCM in Growth failure Version 1.83	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Fanconi anaemia
Red FANCM in Fetal anomalies Version 1.465	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Fanconi anaemia
Amber FANCM in IBMDx study Version 0.38	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber IBMDx Study Victorian Clinical Genetics Services Phenotypes FA-like syndromes, chemotherapy toxicity
Red FANCM in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category C gene Expert Review Red Phenotypes Fanconi anaemia
Green FANCM in Infertility and Recurrent Pregnancy Loss Version 1.50	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Premature ovarian failure 15, MIM# 618096 Spermatogenic failure 28, MIM# 618086