LMX1A

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green LMX1A in Mendeliome Version 1.3795	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Deafness, autosomal dominant 7 MIM#601412 non-syndromic hearing loss
Green LMX1A in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.304	2 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Deafness, autosomal dominant 7 MIM#601412 Deafness, autosomal recessive
No list LMX1A in Additional findings_Paediatric Level 2: Screening Version 0.278	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert list Phenotypes Deafness MIM#601412
Red LMX1A in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.141	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert list Phenotypes Deafness, autosomal dominant 7 MIM#601412

4 panels