KITLG

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green KITLG in Mendeliome Version 1.3513	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Deafness, autosomal dominant 69, unilateral or asymmetric, MIM# 616697 deafness heterochromia iridis hypopigmentation of the skin hyperpigmentation of the skin Waardenburg syndrome,MONDO:0018094, KITLG-related
Green KITLG in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.238	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Waardenburg syndrome, MONDO:0018094, KITLG-related Deafness, autosomal dominant 69, unilateral or asymmetric, MIM# 616697
Amber KITLG in Deafness_Isolated Level 2: Hearing and ear disorders Version 1.82	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert list Expert list Phenotypes Deafness, autosomal dominant 69, unilateral or asymmetric, MIM# 616697
Green KITLG in Hereditary Pigmentary Disorders Level 2: Dermatological disorders Version 1.3	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Victorian Clinical Genetics Services Phenotypes hyperpigmentation with or without hypopigmentation, familial progressive MONDO:0007771

4 panels