Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5ca4ab0c772b7de119dd7766ad07a814> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B5ca4ab0c772b7de119dd7766ad07a814 hasDbXref "Orphanet:75858" @default.
- B5ca4ab0c772b7de119dd7766ad07a814 type Axiom @default.
- B5ca4ab0c772b7de119dd7766ad07a814 annotatedProperty IAO_0000115 @default.
- B5ca4ab0c772b7de119dd7766ad07a814 annotatedSource MONDO_0012423 @default.
- B5ca4ab0c772b7de119dd7766ad07a814 annotatedTarget "MORM syndrome is characterized by the association of intellectual deficit, truncal obesity, retinal dystrophy and micropenis. It has been described in 14 individuals from a consanguineous family. It is transmitted in an autosomal recessive manner. The causative locus has been mapped to chromosome region 9q34." @default.