HKDC1

hexokinase domain containing 1
OMIM: 617221, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red HKDC1 in Retinal disorders Level 3: Posterior segment abnormalities Level 2: Ophthalmological disorders Version 5.4 Latest signed off version: v5.0 (1 May 2024)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Retinitis pigmentosa 92, OMIM:619614

Panel

Reviews

Mode of inheritance

Details

Level 3: Posterior segment abnormalities
Level 2: Ophthalmological disorders
Version 5.4
Latest signed off version: v5.0 (1 May 2024)

review

BIALLELIC, autosomal or pseudoautosomal