lysosomal associated membrane protein 2
OMIM: 309060, Gene2Phenotype
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| LAMP2 in Dilated Cardiomyopathy
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Glycogen Storage Diseases
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Hypertrophic cardiomyopathy_HCM
                    
                    
                       | 2 reviews | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Mendeliome
                    
                    
                     | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Lysosomal Storage Disorder
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Additional findings_Adult
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Intellectual disability syndromic and non-syndromic
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Limb-Girdle Muscular Dystrophy and Distal Myopathy
                    
                    
                       | 2 reviews | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Rhabdomyolysis and Metabolic Myopathy
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Cardiomyopathy_Paediatric
                    
                    
                       | 2 reviews | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Additional findings_Paediatric
                    
                    
                       | 0 reviews | X-LINKED: hemizygous mutation in males, biallelic mutations in females | Sources
 Phenotypes
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| LAMP2 in Fetal anomalies
                    
                    
                     | 1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females | Sources
 Phenotypes
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| LAMP2 in Genomic newborn screening: BabyScreen+
                    
                    
                       | 3 reviews | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Transplant Co-Morbidity
                    
                    
                       | 0 reviews | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| LAMP2 in Cardiac conduction disease
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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