PPARG

peroxisome proliferator activated receptor gamma
OMIM: 601487, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Red PPARG in Fatty Acid Oxidation Defects Level 2: Metabolic disorders Version 1.14 Component of the following Super Panels: Metabolic Disorders Superpanel Progressive Neurological Conditions	1 review	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services
Green PPARG in Lipodystrophy_Lipoatrophy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.25	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Lipodystrophy, familial partial, type 3, MIM# 604367 MONDO:0011448
Green PPARG in Mendeliome Version 1.3512	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Lipodystrophy, familial partial, type 3, MIM# 604367 MONDO:0011448
Green PPARG in Monogenic Diabetes Level 2: Endocrine disorders Version 0.152 Component of the following Super Panels: Metabolic Disorders Superpanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green NHS GMS Phenotypes Insulin resistance, severe, digenic FPLD3 Obesity, severe, 601665 {Diabetes, type 2}, 125853 Lipodystrophy, familial partial, type 3 Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension Insulin resistance, severe, digenic 604367 [Obesity, resistance to] Lipodystrophy, familial partial, type 3, 604367 Insulin resistance, severe, digenic, 604367 Lipodystrophy, familial partial, type 3 604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3 Carotid intimal medial thickness 1, 609338
Green PPARG in Incidentalome_PREGEN_DRAFT Version 0.43	0 reviews	Unknown	Sources NSW Health Pathology Expert Review Green
Red PPARG in Severe early-onset obesity Level 2: Endocrine disorders Version 1.19	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Genomics England PanelApp Phenotypes Obesity, severe, MIM#601665
Green PPARG in Transplant Co-Morbidity Level 2: Screening Version 0.20	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green NHS GMS Phenotypes FPLD3 Lipodystrophy, familial partial, type 3 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3 Insulin resistance, severe, digenic Obesity, severe, 601665 Carotid intimal medial thickness 1, 609338 Lipodystrophy, familial partial, type 3, 604367 {Diabetes, type 2}, 125853 Lipodystrophy, familial partial, type 3 604367 [Obesity, resistance to] Insulin resistance, severe, digenic 604367 Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension Insulin resistance, severe, digenic, 604367