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Atrial septal defect type 2 (sequence analysis of GATA4 gene)
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Atrioventricular septal defect 3 | Craniometaphyseal dysplasia | Oculodentodigital dysplasia | Palmoplantar keratoderma with congenital alopecia | Erythrokeratodermia variabilis | Syndactyly, type III | Hypoplastic left heart syndrome (sequence analysis o
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Atrioventricular septal defect, partial with heterotaxy syndrome (sequence analysis of CRELD1 gene)
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Attention deficit-hyperactivity disorder (sequence analysis of DRD4 gene)
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Atypical hemolytic uremic syndrom (NGS panel of 14 genes)
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Atypical hemolytic uremic syndrome (deletion/duplication analysis on CFH, CFHR1, CFHR2, CFHR3 and CFHR5 genes)
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Atypical hemolytic uremic syndrome 4 (sequence analysis of CFB gene)
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Atypical hemolytic uremic syndrome type 2 (deletion/duplication analysis on CD46 and CFI genes)
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Atypical hemolytic uremic syndrome type 4 (deletion/duplication analysis of CFB gene)
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Atypical hemolytic uremic syndrome type 5 (sequence analysis of C3 gene)
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Atypical hemolytic uremic syndrome type 5 | Primary immunodeficiency (deletion/duplication analysis of C3 gene)
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Atypical hemolytic-uremic syndrome (deletion/duplication analysis of DGKE gene)
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Atypical hemolytic-uremic syndrome (sequence analysis of CFI gene)
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Atypical hemolytic-uremic syndrome (sequence analysis of DGKE gene)
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Atypical hemolytic-uremic syndrome with anti-factor H antibodies (sequence analysis of CFHR5 gene)
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Atypical mycobacteriosis, susceptibility to (sequence analysis of IL12B gene)
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Atypical Rett syndrome (sequence analysis of NTNG1 gene)
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Auditory neuropathy 1 AD (sequence analysis of DIAPH3 gene)
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Auriculocondylar syndrome 2 (sequence analysis of PLCB4 gene)
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Auriculocondylar syndrome 3 (sequence analysis of EDN1 gene)
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