RINT1

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green RINT1 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Infantile liver failure syndrome 3, MIM# 618641
Amber RINT1 in Hereditary Spastic Paraplegia - paediatric Level 2: Neurology and neurodevelopmental disorders Version 1.76 Component of the following Super Panels: Hereditary Spastic Paraplegia Superpanel Neuromuscular Superpanel Progressive Neurological Conditions	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Infantile liver failure syndrome 3, MIM# 618641 Hereditary spastic paraplegia, MONDO:0019064, RINT1-related
Red RINT1 in NCGC Version 0.2	review	Other	Sources NCGC Phenotypes NA
Green RINT1 in Liver Failure_Paediatric Level 2: Gastroenterological disorders Version 1.24 Component of the following Super Panels: Liverome Superpanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Infantile liver failure syndrome 3, MIM# 618641

4 panels