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Http://dbpedia.org/resource/Al-Gazali-Donnai-Mueller syndrome
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http://dbpedia.org/resource/Al-Gazali-Donnai-Mueller_syndrome
http://dbpedia.org/ontology/abstract Al-Gazali-Donnai-Mueller syndrome, also knAl-Gazali-Donnai-Mueller syndrome, also known as Hirschsprung's disease, hypoplastic nails, and minor dysmorphic features syndrome is a rare and deadly genetic disorder which is characterized by Hirschsprung's disease, nail and distal limb hypoplasia, flat facies, upslanting palpebral fissures, narrow philtrum, high palate, micrognathia and low-set ears. No more new cases have been reported in medical literature since 1988. It is a type of Hirschsprung's syndrome.. It is a type of Hirschsprung's syndrome.
http://dbpedia.org/ontology/alias Hirschsprung's disease, hypoplastic nails, and minor dysmorphic features syndrome
http://dbpedia.org/ontology/wikiPageID 70824761
http://dbpedia.org/ontology/wikiPageLength 2954
http://dbpedia.org/ontology/wikiPageRevisionID 1105565055
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http://dbpedia.org/property/causes http://dbpedia.org/resource/Genetic_mutation +
http://dbpedia.org/property/complications http://dbpedia.org/resource/Death +
http://dbpedia.org/property/duration Life-long
http://dbpedia.org/property/frequency very rare
http://dbpedia.org/property/name Al-Gazali-Donnai-Mueller syndrome
http://dbpedia.org/property/onset Birth
http://dbpedia.org/property/prevention None
http://dbpedia.org/property/prognosis Bad
http://dbpedia.org/property/specialty http://dbpedia.org/resource/Medical_genetics +
http://dbpedia.org/property/symptoms Partial absence of nerves in the intestines, facial dysmorphisms and nail hypoplasia
http://dbpedia.org/property/synonyms Hirschsprung's disease, hypoplastic nails, and minor dysmorphic features syndrome
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rdfs:comment Al-Gazali-Donnai-Mueller syndrome, also knAl-Gazali-Donnai-Mueller syndrome, also known as Hirschsprung's disease, hypoplastic nails, and minor dysmorphic features syndrome is a rare and deadly genetic disorder which is characterized by Hirschsprung's disease, nail and distal limb hypoplasia, flat facies, upslanting palpebral fissures, narrow philtrum, high palate, micrognathia and low-set ears. No more new cases have been reported in medical literature since 1988. It is a type of Hirschsprung's syndrome.. It is a type of Hirschsprung's syndrome.
rdfs:label Al-Gazali-Donnai-Mueller syndrome
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