MCM7

Panel	Reviews	Mode of inheritance	Details
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Red MCM7 in Lipodystrophy_Lipoatrophy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.25	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Syndromic disease, MONDO:0002254, MCM7-related Meier-Gorlin syndrome Microcephaly Intellectual disability Lipodystrophy Adrenal insufficiency
Amber MCM7 in Mendeliome Version 1.3512	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Syndromic disease, MONDO:0002254, MCM7-related Meier-Gorlin syndrome Microcephaly Intellectual disability Lipodystrophy Adrenal insufficiency
Amber MCM7 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.357	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Syndromic disease, MONDO:0002254, MCM7-related Meier-Gorlin syndrome Microcephaly Intellectual disability Lipodystrophy Adrenal insufficiency
Amber MCM7 in Fetal anomalies Version 1.465	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Syndromic disease, MONDO:0002254, MCM7-related Meier-Gorlin syndrome Microcephaly Intellectual disability Lipodystrophy Adrenal insufficiency

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