Genetic Diseases, Inborn PubMed MeSh Term

Overview

subject area of

• ANALYZING THE RELATIONSHIP BETWEEN AGE AT ONSET AND RISK TO RELATIVES  Journal Article
• Molecular consequences of the R453C hypertrophic cardiomyopathy mutation on human β-cardiac myosin motor function  Journal Article

broader concept

• Congenital, Hereditary, and Neonatal Diseases and Abnormalities  PubMed MeSh Term

narrower concept

• Genetic Diseases, Inborn - Cardiomyopathy, Hypertrophic, Familial  PubMed MeSh Term
• Genetic Diseases, Inborn - Chromosome Disorders  PubMed MeSh Term
• Genetic Diseases, Inborn - Cystic Fibrosis  PubMed MeSh Term
• Genetic Diseases, Inborn - Dwarfism  PubMed MeSh Term
• Genetic Diseases, Inborn - Eye Diseases, Hereditary  PubMed MeSh Term
• Genetic Diseases, Inborn - Kallmann Syndrome  PubMed MeSh Term
• Genetic Diseases, Inborn - Kartagener Syndrome  PubMed MeSh Term
• Genetic Diseases, Inborn - Metabolism, Inborn Errors  PubMed MeSh Term
• Genetic Diseases, Inborn - Muscular Dystrophies  PubMed MeSh Term
• Genetic Diseases, Inborn - Osteochondrodysplasias  PubMed MeSh Term
• Genetic Diseases, Inborn - Primary Immunodeficiency Diseases  PubMed MeSh Term
• Genetic Diseases, Inborn - Werner Syndrome  PubMed MeSh Term