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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 wikiPageRevisionID "596327948".
- Branchio-oculo-facial_syndrome name "Branchio-oculo-facial syndrome".
- Branchio-oculo-facial_syndrome omim "113620".
- Branchio-oculo-facial_syndrome subject Category:Genetic_disorders.
- Branchio-oculo-facial_syndrome subject Category:Transcription_factor_deficiencies.
- Branchio-oculo-facial_syndrome type Disease.
- Branchio-oculo-facial_syndrome type Situation.
- 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 m.0zn1h2g.
- Branchio-oculo-facial_syndrome sameAs Q17022522.
- Branchio-oculo-facial_syndrome sameAs Q17022522.
- Branchio-oculo-facial_syndrome wasDerivedFrom Branchio-oculo-facial_syndrome?oldid=596327948.
- Branchio-oculo-facial_syndrome isPrimaryTopicOf Branchio-oculo-facial_syndrome.