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Otopalatodigital syndrome
MONDO:0019027A form of frontootopalatodigital syndrome, characterized by deafness, cleft palate, and characteristic digital anomalies. OPD syndrome is divided into two forms based on severity: the milder form designated OPD type 1 (OPD1), and the more severe and often lethal form designated OPD type 2 (OPD2). OPD is an X-linked disorder. Two other genetic disorders with features overlapping OPD, frontometaphyseal dysplasia (FMD) and osteodysplasty, Melnick-Needles type (MNS) have been described; thus OPD1, OPD2, FMD, and MNS are allelic disorders.
Also known as: oto-palatal-digital syndrome, oto-palato-digital syndrome, type 2 (Andre syndrome)
0 clinical trials for this condition and its sub-types, 0 tagged with Otopalatodigital syndrome itself.
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Browse by category →Sub-types of Otopalatodigital syndrome
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Otopalatodigital syndrome type 1 0 trials
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Otopalatodigital syndrome type 2 0 trials
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