Laurence–Moon syndrome

CaLiGraph

Property	Value
rdf:type	owl:NamedIndividual Eponymous disease Genetic disorder with OMIM but no gene Rare disease Syndrome affecting the eye Autosomal recessive disorder Congenital disorder MeSH code (C10) MeSH code (C16)
rdfs:label	Laurence–Moon syndrome
owl:sameAs	dbr:Laurence–Moon_syndrome
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Rare_diseases http://en.wikipedia.org/wiki/List_of_eponymous_diseases http://en.wikipedia.org/wiki/List_of_syndromes http://en.wikipedia.org/wiki/Gonadotropin-releasing_hormone_insensitivity http://en.wikipedia.org/wiki/Category:Genetic_disorders_with_OMIM_but_no_gene http://en.wikipedia.org/wiki/Category:Syndromes_affecting_the_eye http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C10) http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16) http://en.wikipedia.org/wiki/List_of_congenital_disorders http://en.wikipedia.org/wiki/Category:Autosomal_recessive_disorders
skos:prefLabel	Laurence–Moon syndrome
skos:altLabel	laurence-moon syndrome
clgo:diseasesDB	30072
clgo:icd10	Q87.8
clgo:icd9	759.89
clgo:meshId	D007849
clgo:omim	245800
clgo:orpha	2377

About: clgr:Laurence–Moon_syndrome