WD repeat domain 45
OMIM: 300526, Gene2Phenotype
| Panel | Reviews | Mode of inheritance | Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| WDR45 in Early-onset Dementia
                    
                    
                       | 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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| WDR45 in Early-onset Parkinson 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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| WDR45 in Angelman Rett like syndromes
                    
                    
                       | 1 review | Other | Sources
 Phenotypes
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| WDR45 in Brain Calcification
                    
                    
                       | 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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| WDR45 in Cerebral Palsy
                    
                    
                       | 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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| WDR45 in Mendeliome
                    
                    
                     | 2 reviews | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Sources
 Phenotypes
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| WDR45 in Lysosomal Storage Disorder
                    
                    
                       | 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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| WDR45 in Genetic Epilepsy
                    
                    
                       | 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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| WDR45 in Regression
                    
                    
                       | 0 reviews | Unknown | Sources
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| WDR45 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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| WDR45 in Dystonia - complex
                    
                    
                       | 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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| WDR45 in Neurodegeneration with brain iron accumulation
                    
                    
                       | 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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| WDR45 in Miscellaneous Metabolic Disorders
                    
                    
                       | 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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| WDR45 in Fetal anomalies
                    
                    
                     | 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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