C16orf62

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Amber C16orf62 in Anophthalmia_Microphthalmia_Coloboma Level 2: Ophthalmological disorders Version 1.50	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135 Tags new gene name
Amber C16orf62 in Chondrodysplasia Punctata Level 2: Skeletal disorders Version 1.1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert list Phenotypes Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135
Green C16orf62 in Mendeliome Version 1.3512	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135 Tags new gene name
Green C16orf62 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 Green Expert list Phenotypes Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135 Tags new gene name
Green C16orf62 in Fetal anomalies Version 1.465	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135

5 panels