SPRY4

Panel	Reviews	Mode of inheritance	Details
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Amber SPRY4 in Differences of Sex Development Level 2: Dysmorphic and congenital abnormality syndromes Version 0.293	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert list Phenotypes Hypogonadotropic hypogonadism 17 with or without anosmia, MIM# 615266 Tags disputed
Amber SPRY4 in Mendeliome Version 1.1902	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Hypogonadotropic hypogonadism 17 with or without anosmia, MIM# 615266 Tags disputed
Red SPRY4 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.522	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Hypogonadotropic hypogonadism 17 with or without anosmia, MIM# 615266

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