Structural eye disease
Gene: ARL13B
retinal gene, can't find any evidence that it is associated with structural eye diseaseCreated: 19 Jun 2019, 3:32 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Joubert syndrome 8; 612291
Publications
Submitted on behalf of Professor Nicola Ragge (Wessex and West Midlands GLH). retinal gene, can't find any evidence that it is associated with structural eye diseaseCreated: 17 Apr 2019, 3:30 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Joubert syndrome 8 612291
Publications
Phenotypes for gene: ARL13B were changed from Joubert syndrome 8 612291; Joubert syndrome 8 to Joubert syndrome 8 612291
Source NHS GMS was added to ARL13B. Added phenotypes Joubert syndrome 8 612291 for gene: ARL13B Publications for gene ARL13B were changed from 18674751; 25138100 to 25138100; 18674751
gene: ARL13B was added gene: ARL13B was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: ARL13B was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ARL13B were set to 18674751; 25138100 Phenotypes for gene: ARL13B were set to Joubert syndrome 8