SLC27A3:Ensemblv90

solute carrier family 27 member 3
OMIM: 604193, ClinGen, DECIPHER

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Red SLC27A3 in Mendeliome Version 1.3802	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Inherited neurodegenerative disorder, MONDO:0024237, SLC27A3-related
Red SLC27A3 in Optic Atrophy Level 2: Ophthalmological disorders Version 1.65 Component of the following Super Panels: Retinal Disorders Superpanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Literature Phenotypes Inherited neurodegenerative disorder, MONDO:0024237, SLC27A3-related
Red SLC27A3 in Regression Level 2: Neurology and neurodevelopmental disorders Version 0.601	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Literature Phenotypes Inherited neurodegenerative disorder, MONDO:0024237, SLC27A3-related
Red SLC27A3 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.508	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Literature Phenotypes Inherited neurodegenerative disorder, MONDO:0024237, SLC27A3-related
Red SLC27A3 in Ataxia Level 2: Neurology and neurodevelopmental disorders Version 1.162 Component of the following Super Panels: Ataxia_Superpanel Neuromuscular Superpanel Progressive Neurological Conditions	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Literature Phenotypes Inherited neurodegenerative disorder, MONDO:0024237, SLC27A3-related
Red SLC27A3 in Neurodegeneration with brain iron accumulation Level 2: Neurology and neurodevelopmental disorders Version 1.3 Component of the following Super Panels: Progressive Neurological Conditions	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Literature Phenotypes Inherited neurodegenerative disorder, MONDO:0024237, SLC27A3-related
Red SLC27A3 in Neurodegeneration with brain iron accumulation Level 2: Neurology and neurodevelopmental disorders Version 2.0	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Literature Literature Expert Review Red Phenotypes Inherited neurodegenerative disorder, MONDO:0024237, SLC27A3-related