Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Branchio-oculo-facial_syndrome> ?p ?o }
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- Branchio-oculo-facial_syndrome abstract "Branchio-oculo-facial syndrome (BOFS) is a disease that arises from a mutation in the TFAP2A gene. It is a rare autosomal dominant disorder that starts to affect a child's development before birth. Symptoms of this condition include skin abnormalities on the neck, deformities of the ears and eyes, and other distinctive facial features such a cleft lip along with slow growth, mental retardation and premature graying of hair.".
- Branchio-oculo-facial_syndrome omim "113620".
- Branchio-oculo-facial_syndrome wikiPageID "41341790".
- Branchio-oculo-facial_syndrome wikiPageLength "5445".
- Branchio-oculo-facial_syndrome wikiPageOutDegree "23".
- Branchio-oculo-facial_syndrome wikiPageRevisionID "675787266".
- Branchio-oculo-facial_syndrome wikiPageWikiLink Amino_acid.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Apoptosis.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Branchial_arch.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Branchio-oto-renal_syndrome.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Category:Genetic_disorders.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Category:Transcription_factor_deficiencies.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Cell_division.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Cleft_lip_and_palate.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Dominance_(genetics).
- Branchio-oculo-facial_syndrome wikiPageWikiLink Embryo.
- Branchio-oculo-facial_syndrome wikiPageWikiLink G262E.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Hypertelorism.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Intellectual_disability.
- Branchio-oculo-facial_syndrome wikiPageWikiLink L249P.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Middle_ear.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Penetrance.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Proline.
- Branchio-oculo-facial_syndrome wikiPageWikiLink R254W.
- Branchio-oculo-facial_syndrome wikiPageWikiLink R255G.
- Branchio-oculo-facial_syndrome wikiPageWikiLink TFAP2A.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Transcription_factor.
- Branchio-oculo-facial_syndrome wikiPageWikiLink Visual_impairment.
- Branchio-oculo-facial_syndrome wikiPageWikiLinkText "Branchio-oculo-facial syndrome".
- Branchio-oculo-facial_syndrome name "Branchio-oculo-facial syndrome".
- Branchio-oculo-facial_syndrome omim "113620".
- Branchio-oculo-facial_syndrome wikiPageUsesTemplate Template:Clarify.
- Branchio-oculo-facial_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Branchio-oculo-facial_syndrome wikiPageUsesTemplate Template:Mcn.
- Branchio-oculo-facial_syndrome wikiPageUsesTemplate Template:Reflist.
- Branchio-oculo-facial_syndrome subject Category:Genetic_disorders.
- Branchio-oculo-facial_syndrome subject Category:Transcription_factor_deficiencies.
- Branchio-oculo-facial_syndrome hypernym Disease.
- Branchio-oculo-facial_syndrome type Disease.
- Branchio-oculo-facial_syndrome type Thing.
- Branchio-oculo-facial_syndrome type Q12136.
- Branchio-oculo-facial_syndrome comment "Branchio-oculo-facial syndrome (BOFS) is a disease that arises from a mutation in the TFAP2A gene. It is a rare autosomal dominant disorder that starts to affect a child's development before birth. Symptoms of this condition include skin abnormalities on the neck, deformities of the ears and eyes, and other distinctive facial features such a cleft lip along with slow growth, mental retardation and premature graying of hair.".
- Branchio-oculo-facial_syndrome label "Branchio-oculo-facial syndrome".
- Branchio-oculo-facial_syndrome sameAs Q17022522.
- Branchio-oculo-facial_syndrome sameAs m.0zn1h2g.
- Branchio-oculo-facial_syndrome sameAs Q17022522.
- Branchio-oculo-facial_syndrome wasDerivedFrom Branchio-oculo-facial_syndrome?oldid=675787266.
- Branchio-oculo-facial_syndrome isPrimaryTopicOf Branchio-oculo-facial_syndrome.