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- Bc65ef16b853fc858f764747afd03c7c5 hasDbXref "Orphanet:952" @default.
- Bc65ef16b853fc858f764747afd03c7c5 type Axiom @default.
- Bc65ef16b853fc858f764747afd03c7c5 annotatedProperty IAO_0000115 @default.
- Bc65ef16b853fc858f764747afd03c7c5 annotatedSource MONDO_0008673 @default.
- Bc65ef16b853fc858f764747afd03c7c5 annotatedTarget "Acrofacialdysostosis, Weyers type (WAD) is a rare ectodermal dysplasia syndrome with bone abnormalities characterized by onychodystrophy; anomalies of the lower jaw, oral vestibule and dentition; post-axialpolydactyly; moderately restricted growth with short limbs; and normal intelligence. Although it closely resembles Ellis-van Creveld syndrome, an allelic disorder and another type of ciliopathy, WAD is usually a milder disease without the presence of heart abnormalities and is inherited in an autosomal dominant manner." @default.