Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B53d5bcf80cfaa8dfea872ab82f7c6cb8> ?p ?o ?g. }
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- B53d5bcf80cfaa8dfea872ab82f7c6cb8 hasDbXref "Orphanet:168782" @default.
- B53d5bcf80cfaa8dfea872ab82f7c6cb8 hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B53d5bcf80cfaa8dfea872ab82f7c6cb8 type Axiom @default.
- B53d5bcf80cfaa8dfea872ab82f7c6cb8 annotatedProperty IAO_0000115 @default.
- B53d5bcf80cfaa8dfea872ab82f7c6cb8 annotatedSource MONDO_0015681 @default.
- B53d5bcf80cfaa8dfea872ab82f7c6cb8 annotatedTarget "A rare pervasive developmental disorder with a disease onset before the age of three and characterized by a dramatic loss of behavioral and developmental functioning after atleast two years of normal development. Manifestations of the disease include loss of speech, incontinence, communication and social interaction problems, stereotypical autistic behaviors and dementia." @default.