MCM7

Panel	Reviews	Mode of inheritance	Details
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Red MCM7 in Lipodystrophy_Lipoatrophy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.17	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Meier-Gorlin syndrome Microcephaly Intellectual disability Lipodystrophy Adrenal insufficiency
Amber MCM7 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Meier-Gorlin syndrome Microcephaly Intellectual disability Lipodystrophy Adrenal insufficiency
Amber MCM7 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.269	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Meier-Gorlin syndrome Microcephaly Intellectual disability Lipodystrophy Adrenal insufficiency
Amber MCM7 in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Meier-Gorlin syndrome Microcephaly Intellectual disability Lipodystrophy Adrenal insufficiency

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