About: Al-Gazali-Donnai-Mueller syndrome

An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org:8891

Al-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.

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dbo:abstract
  • Al-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. (en)
dbo:alias
  • (en)
  • Hirschsprung's disease, hypoplastic nails, and minor dysmorphic features syndrome (en)
dbo:wikiPageID
  • 70824761 (xsd:integer)
dbo:wikiPageLength
  • 2954 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID
  • 1105565055 (xsd:integer)
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dbp:causes
dbp:complications
dbp:duration
  • Life-long (en)
dbp:frequency
  • very rare (en)
dbp:name
  • Al-Gazali-Donnai-Mueller syndrome (en)
dbp:onset
  • Birth (en)
dbp:prevention
  • None (en)
dbp:prognosis
  • Bad (en)
dbp:specialty
dbp:symptoms
  • Partial absence of nerves in the intestines, facial dysmorphisms and nail hypoplasia (en)
dbp:synonyms
  • Hirschsprung's disease, hypoplastic nails, and minor dysmorphic features syndrome (en)
dbp:wikiPageUsesTemplate
dcterms:subject
rdf:type
rdfs:comment
  • Al-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. (en)
rdfs:label
  • Al-Gazali-Donnai-Mueller syndrome (en)
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