FMN1

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Amber FMN1 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes oligosyndactyly radioulnar synostosis hearing loss renal defects Tags SV/CNV
Red FMN1 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.285	review	Unknown	Sources Expert Review Amber Literature Expert Review Red Expert list Emory Genetics Laboratory UKGTN Phenotypes Animal models with skeletal dysplastic phenotypes
Amber FMN1 in Hand and foot malformations Level 2: Dysmorphic and congenital abnormality syndromes Version 0.74 Component of the following Super Panels: Limb and Digital Malformations SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert list Phenotypes oligosyndactyly radioulnar synostosis hearing loss renal defects Tags SV/CNV
Amber FMN1 in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes oligosyndactyly radioulnar synostosis hearing loss renal defects

4 panels