ZMYND10

zinc finger MYND-type containing 10
OMIM: 607070, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green ZMYND10 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.430	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Phenotypes Primary ciliary dyskinesia 22 MONDO:0014192
Green ZMYND10 in Ciliary Dyskinesia Level 2: Respiratory disorders Version 1.40	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 22, MIM#615444
Green ZMYND10 in Heterotaxy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.36	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 22, MIM#615444
Green ZMYND10 in Mendeliome Version 1.2302	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 22, MIM#615444
Green ZMYND10 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Ciliary dyskinesia, primary, 22, 615444 (3)
Green ZMYND10 in Fetal anomalies Version 1.313	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 22, MIM#615444
Green ZMYND10 in Prepair 1000+ Level 2: Screening Version 1.1566	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Ciliary dyskinesia, primary, 22 (MIM#615444)