Stickler syndrome - CaLiGraph

CaLiGraph

Property	Value
rdf:type	owl:NamedIndividual Autosomal dominant disorder Rare syndrome Congenital disorder Eye disease
rdfs:label	Stickler syndrome
owl:sameAs	dbr:Stickler_syndrome
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Causes_of_hearing_loss http://en.wikipedia.org/wiki/Micrognathism http://en.wikipedia.org/wiki/Sensorineural_hearing_loss http://en.wikipedia.org/wiki/Cleft_lip_and_cleft_palate http://en.wikipedia.org/wiki/Stickler_syndrome http://en.wikipedia.org/wiki/Category:Autosomal_dominant_disorders http://en.wikipedia.org/wiki/List_of_syndromes http://en.wikipedia.org/wiki/Chromosome_6 http://en.wikipedia.org/wiki/Marfan_syndrome http://en.wikipedia.org/wiki/Category:Rare_syndromes http://en.wikipedia.org/wiki/Chromosome_1 http://en.wikipedia.org/wiki/Connective_tissue_disease http://en.wikipedia.org/wiki/Collagen,_type_II,_alpha_1 http://en.wikipedia.org/wiki/Myalgia http://en.wikipedia.org/wiki/Deafblindness http://en.wikipedia.org/wiki/List_of_congenital_disorders http://en.wikipedia.org/wiki/Category:Eye_diseases http://en.wikipedia.org/wiki/Chromosome_12
skos:prefLabel	Stickler syndrome
skos:altLabel	Stickler Syndrome Sticklers Syndrome
clgo:diseasesDB	29327
clgo:icd10	Q89.8
clgo:icd9	759.89
clgo:omim	108300
is clgo:knownFor of	Gunnar B. Stickler

About: clgr:Stickler_syndrome