Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bc6f03cf0acab5e6b7c48cdcc4d5cd2e6> ?p ?o ?g. }
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- Bc6f03cf0acab5e6b7c48cdcc4d5cd2e6 hasDbXref "NCIT:C84522" @default.
- Bc6f03cf0acab5e6b7c48cdcc4d5cd2e6 type Axiom @default.
- Bc6f03cf0acab5e6b7c48cdcc4d5cd2e6 annotatedProperty IAO_0000115 @default.
- Bc6f03cf0acab5e6b7c48cdcc4d5cd2e6 annotatedSource MONDO_0011147 @default.
- Bc6f03cf0acab5e6b7c48cdcc4d5cd2e6 annotatedTarget "A condition in which some or all of the cells of the body contain extra genetic material from chromosome 18. Clinical features of this condition may include the following: spina bifida, hearing loss, cleft lip, cleft palate, undescended testes, rocker bottom feet, micrognathia, low set ears, cardiac anomalies (ventricular septal defect, atrial septal defect, patent ductus arteriosus, tetralogy of Fallot), intellectual disability, holoprosencephaly, pituitary dysplasia, seizures, autoimmune disorders, hip dysplasia, and/or congenital cataracts." @default.