MIR17HG

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green MIR17HG in Mendeliome Version 1.1891	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Feingold syndrome 2 OMIM #614326
Green MIR17HG in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Expert list Phenotypes Feingold syndrome 2 OMIM #614326 Tags SV/CNV
Green MIR17HG in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.285	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
Amber MIR17HG in Fetal anomalies Version 1.255	review	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

4 panels