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- Johnson–McMillin_syndrome abstract "Johnson–McMillin syndrome is a neuroectodermal syndrome that consist of conductive hearing loss and microtia.".
- Johnson–McMillin_syndrome wikiPageID "25477282".
- Johnson–McMillin_syndrome wikiPageRevisionID "569631096".
- Johnson–McMillin_syndrome name "Johnson–McMillin syndrome".
- Johnson–McMillin_syndrome omim "147770".
- Johnson–McMillin_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Johnson–McMillin_syndrome subject Category:Genodermatoses.
- Johnson–McMillin_syndrome type Disease.
- Johnson–McMillin_syndrome type Situation.
- Johnson–McMillin_syndrome comment "Johnson–McMillin syndrome is a neuroectodermal syndrome that consist of conductive hearing loss and microtia.".
- Johnson–McMillin_syndrome label "Johnson–McMillin syndrome".
- Johnson–McMillin_syndrome sameAs Johnson%E2%80%93McMillin_syndrome.
- Johnson–McMillin_syndrome sameAs Q16940647.
- Johnson–McMillin_syndrome sameAs Q16940647.
- Johnson–McMillin_syndrome wasDerivedFrom Johnson–McMillin_syndrome?oldid=569631096.