NUF2

Panel	Reviews	Mode of inheritance	Details
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Red NUF2 in Mendeliome Version 1.3512	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes microcephaly short stature bilateral vocal cord paralysis micrognathia atrial septal defect
Red NUF2 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.357	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes microcephaly short stature bilateral vocal cord paralysis micrognathia atrial septal defect
Red NUF2 in Fetal anomalies Version 1.465	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert Review Phenotypes Syndromic disease, MONDO:0002254 microcephaly short stature bilateral vocal cord paralysis micrognathia atrial septal defect

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