SPEF2

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Amber SPEF2 in Ciliary Dyskinesia Level 2: Respiratory disorders Version 1.39	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Spermatogenic failure 43, MIM#618751 Primary ciliary dyskinesia-like phenotype
Green SPEF2 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Spermatogenic failure 43, MIM#618751 Spermatogenic failure 43, MIM#618751 Primary ciliary dyskinesia-like phenotype
Red SPEF2 in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Spermatogenic failure 43, MIM#618751 Primary ciliary dyskinesia-like phenotype

3 panels