PLIN1

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Amber PLIN1 in Lipodystrophy_Lipoatrophy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.25	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Lipodystrophy, familial partial, type 4, MIM# 613877 Tags disputed
Amber PLIN1 in Mendeliome Version 1.3499	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Lipodystrophy, familial partial, type 4, MIM# 613877 Tags disputed
Amber PLIN1 in Monogenic Diabetes Level 2: Endocrine disorders Version 0.152 Component of the following Super Panels: Metabolic Disorders Superpanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber NHS GMS Phenotypes Lipodystrophy, familial partial, type 4, 613877 Severe insulin resistance, partial lipodystrophy and diabetes Tags disputed

3 panels