Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B9b9add77411c07bfb55d063500571b05> ?p ?o ?g. }
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- B9b9add77411c07bfb55d063500571b05 hasDbXref "Orphanet:2266" @default.
- B9b9add77411c07bfb55d063500571b05 type Axiom @default.
- B9b9add77411c07bfb55d063500571b05 annotatedProperty IAO_0000115 @default.
- B9b9add77411c07bfb55d063500571b05 annotatedSource MONDO_0016414 @default.
- B9b9add77411c07bfb55d063500571b05 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.