Obesity, susceptibility to, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (ADRB3 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, susceptibility to, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (UCP1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, severe, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (PPARG gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, mild, early-onset, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (NR0B2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, late-onset, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (AGRP gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, susceptibility to, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (GHRL gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, susceptibility to, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (ENPP1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, autosomal dominant, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - D Deletion/duplication analysis
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Obesity, association with, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (SDC3 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, early-onset, susceptibility to, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (POMC gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, variation in, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (PPARGC1B gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, susceptibility to, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (ADRB2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, severe, and type II diabetes, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (UCP3 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, severe, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - D Deletion/duplication analysis
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Obesity, susceptibility to, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (CARTPT gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Obesity, early-onset, susceptibility to, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - D Deletion/duplication analysis
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Obesity, autosomal dominant, 601665, Autosomal recessive, Autosomal dominant, Multifactorial (Obesity due to pro-opiomelanocortin deficiency) (MC4R gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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MC4R gene, obesity Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile | 1 | 1 | - C Sequence analysis of the entire coding region
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Invitae Expanded Renal Disease Panel Invitae
United States | 693 | 388 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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Infertility Panel Centogene AG - the Rare Disease Company
Germany | 243 | 238 | - D Deletion/duplication analysis
- E Sequence analysis of select exons
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
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