RNH1

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red RNH1 in Cataract Level 2: Ophthalmological disorders Version 0.375	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Neurodevelopmental disorder, MONDO:0700092, RNH1-related
Green RNH1 in Mendeliome Version 1.3512	4 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Encephalopathy, acute, infection-induced, susceptibility to, 12 MIM#620461
Green RNH1 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.267 Component of the following Super Panels: Progressive Neurological Conditions	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Encephalopathy, acute, infection-induced, susceptibility to, 12 MIM#620461
Green RNH1 in Regression Level 2: Neurology and neurodevelopmental disorders Version 0.594	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder, MONDO:0700092, RNH1-related {Encephalopathy, acute, infection-induced, susceptibiliyt to, 12}, MIM# 620461
Red RNH1 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Neurodevelopmental disorder, MONDO:0700092, RNH1-related

5 panels