ISCA-37486-Loss

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green ISCA-37486-Loss Region in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.250	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Expert Review Green Expert list Phenotypes Chromosome 16p11.2 deletion syndrome, MIM#611913, distal BP2-BP3 intellectual disability autism obesity Tags SV/CNV
Green ISCA-37486-Loss Region in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.780	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Expert Review Green Expert list Phenotypes Chromosome 16p11.2 deletion syndrome, MIM#611913, distal BP2-BP3 intellectual disability autism obesity Tags SV/CNV
Green ISCA-37486-Loss Region in Common deletion and duplication syndromes Version 0.158	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Chromosome 16p11.2 deletion syndrome, MIM#611913, distal BP2-BP3 intellectual disability autism obesity Tags SV/CNV
Green ISCA-37486-Loss Region in Severe early-onset obesity Level 2: Endocrine disorders Version 1.32	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Expert Review Green Expert list Phenotypes Chromosome 16p11.2 deletion syndrome, MIM#611913, distal BP2-BP3 intellectual disability autism obesity Tags SV/CNV