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Total number of diseases with letter "O" in database: 156

A -B -C -D -E -F -G -H -I -J -K -L -M -N -O -P -Q -R -S -T -U -V -W -X -Y - Z

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Records: 76 - 90

76: Opitz-G syndrome, TYPE II (OGS2)
77: OPMD
78: OPMD, autosomal recessive
79: Opsin 2 (OPN2)
80: Optic atrophy 1 gene; OPA1
81: OPTIC ATROPHY 3, AUTOSOMAL DOMINANT
82: Optic Atrophy Type 1 and DeafnessClinical Tests 31105931
83: Optic Atrophy Type 1 and DeafnessClinical Tests 31105931
84: Optic atrophy, deafness, ophthalmoplegia, and myopathy
85: Optic coloboma, vesicoureteral reflux, and renal anomalies
86: Optic nerve coloboma with renal disease
87: Opticoacoustic nerve atrophy with dementia
88: Oral-facial digital syndrome, type I
89: Oregon type tyrosinemia
90: Ornithine aminotransferase (OAT)

Should you not find the disease for which you are searching, please send an email to EDDNAL: eddnal@skypro.be

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