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- B11de4815b8d16ef99bedc60de93ecee0 hasDbXref "Orphanet:250999" @default.
- B11de4815b8d16ef99bedc60de93ecee0 type Axiom @default.
- B11de4815b8d16ef99bedc60de93ecee0 annotatedProperty IAO_0000115 @default.
- B11de4815b8d16ef99bedc60de93ecee0 annotatedSource MONDO_0012927 @default.
- B11de4815b8d16ef99bedc60de93ecee0 annotatedTarget "1q41q42 microdeletion syndrome is a chromosomal anomaly characterized by a severe developmental delay and/or intellectual disability, typical facial dysmorphic features, brain anomalies, seizures, cleft palate, clubfeet, nail hypoplasia and congenital heart disease." @default.