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- Ba87499078c9c50b55b5804124a6daad0 hasDbXref "Orphanet:2266" @default.
- Ba87499078c9c50b55b5804124a6daad0 type Axiom @default.
- Ba87499078c9c50b55b5804124a6daad0 annotatedProperty IAO_0000115 @default.
- Ba87499078c9c50b55b5804124a6daad0 annotatedSource MONDO_0016414 @default.
- Ba87499078c9c50b55b5804124a6daad0 annotatedTarget "A syndrome characterized by hypotrichosis, syndactyly, intellectual deficit and early eruption of teeth. It has been described in two patients. The mode of transmission appears to be autosomal recessive." @default.