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D-2-hydroxyglutaric aciduria (deletion/duplication analysis on D2HGDH gene)
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D-2-hydroxyglutaric aciduria (sequence analysis of D2HGDH gene)
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D-2-hydroxyglutaric aciduria 2 (sequence analysis of IDH2 gene)
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Danon disease (sequence analysis of LAMP2 gene)
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Darier disease (sequence analysis of ATP2A2 gene)
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Darier-White disease (deletion/duplication analysis on ATP2A2 gene)
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Deafness (sequence analysis of OTOF gene)
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Deafness and male infertility (sequence analysis of CATSPER2 gene)
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Deafness autosomal dominant 13 | Deafness autosomal recessive 53 | Fibrochondrogenesis 2 | Stickler type 3 syndrome | Weissenbacher-Zweymuller syndrome (deletion/duplication analysis on COL11A2 gene)
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Deafness autosomal dominant 13 | Deafness autosomal recessive 53 | Fibrochondrogenesis 2 | Stickler type 3 syndrome | Weissenbacher-Zweymuller syndrome (sequence analysis of COL11A2 gene)
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Deafness nonsyndromic sensorineural mitochondrial (sequence analysis of MT-RNR1 gene)
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Deafness, autosomal dominant 1 (sequence analysis of DIAPH1 gene)
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Deafness, autosomal dominant 10 (sequence analysis of EYA4 gene)
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Deafness, autosomal dominant 12 (sequence analysis of TECTA gene)
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Deafness, autosomal dominant 15 (sequence analysis of POU4F3 gene)
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Deafness, autosomal dominant 20/26 (sequence analysis of ACTG1 gene)
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Deafness, autosomal dominant 22 (sequence analysis of MYO6 gene)
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Deafness, autosomal dominant 23 (sequence analysis of SIX1 gene)
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Deafness, autosomal dominant 25 (sequence analysis of SLC17A8 gene)
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Deafness, autosomal dominant 28 (sequence analysis of GRHL2 gene)
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