Mowat–Wilson syndrome

CaLiGraph

Property	Value
rdf:type	Syndrome affecting the heart Syndrome with craniofacial abnormalities owl:NamedIndividual Eponymous disease Rare genetic syndrome Syndrome affecting the nervous system Syndrome affecting the gastrointestinal tract Syndrome with intellectual disability Transcription factor deficiency
rdfs:label	Mowat–Wilson syndrome
owl:sameAs	dbr:Mowat–Wilson_syndrome
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Syndromes_affecting_the_gastrointestinal_tract http://en.wikipedia.org/wiki/Category:Rare_genetic_syndromes http://en.wikipedia.org/wiki/List_of_eponymous_diseases http://en.wikipedia.org/wiki/List_of_syndromes http://en.wikipedia.org/wiki/Hirschsprung's_disease http://en.wikipedia.org/wiki/Category:Syndromes_affecting_the_heart http://en.wikipedia.org/wiki/Category:Syndromes_with_craniofacial_abnormalities http://en.wikipedia.org/wiki/Agenesis_of_the_corpus_callosum http://en.wikipedia.org/wiki/Category:Syndromes_affecting_the_nervous_system http://en.wikipedia.org/wiki/Facies_(medical) http://en.wikipedia.org/wiki/Angelman_syndrome http://en.wikipedia.org/wiki/Category:Syndromes_with_intellectual_disability http://en.wikipedia.org/wiki/Category:Transcription_factor_deficiencies http://en.wikipedia.org/wiki/Ciliopathy
skos:prefLabel	Mowat–Wilson syndrome
clgo:differentialDiagnosis	Angelman syndrome
clgo:diseasesDB	32975
clgo:icd10	Q43.1
clgo:meshId	C536990
clgo:omim	235730
clgo:orpha	2152
clgo:treatment	Symptomatic treatment

About: clgr:Mowat–Wilson_syndrome