MIR17HG

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green MIR17HG in Mendeliome Version 1.3499	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Feingold syndrome 2 OMIM #614326 Tags non-coding gene
Green MIR17HG in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.398	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Expert list Phenotypes Feingold syndrome 2 OMIM #614326 Tags SV/CNV non-coding gene
Green MIR17HG in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.346	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Radboud University Medical Center, Nijmegen Expert list NHS GMS Expert list Phenotypes FS2 Microcephaly-oculo-digito-esophageal-duodenal syndrome Brachydactyly with short stature and microcephaly Feingold syndrome 2, 614326 Tags non-coding gene
Amber MIR17HG in Fetal anomalies Version 1.465	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Genomics England PanelApp Expert list Expert list Phenotypes Feingold syndrome 2, MIM #614326 Tags SV/CNV non-coding gene

4 panels