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- B0ef2f0aab80f29aaace77679752a5adf hasDbXref "Orphanet:669" @default.
- B0ef2f0aab80f29aaace77679752a5adf hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B0ef2f0aab80f29aaace77679752a5adf type Axiom @default.
- B0ef2f0aab80f29aaace77679752a5adf annotatedProperty IAO_0000115 @default.
- B0ef2f0aab80f29aaace77679752a5adf annotatedSource MONDO_0019027 @default.
- B0ef2f0aab80f29aaace77679752a5adf annotatedTarget "A 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." @default.