Pfeiffer syndrome - CaLiGraph

Property	Value
rdf:type	owl:NamedIndividual Rare syndrome Skin condition Syndrome with dysmelia Congenital disorder Cell surface receptor deficiency
rdfs:label	Pfeiffer syndrome
owl:sameAs	dbr:Pfeiffer_syndrome
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Congenital_disorders http://en.wikipedia.org/wiki/Saethre%E2%80%93Chotzen_syndrome http://en.wikipedia.org/wiki/Chromosome_10 http://en.wikipedia.org/wiki/List_of_diseases_(M) http://en.wikipedia.org/wiki/List_of_diseases_(P) http://en.wikipedia.org/wiki/List_of_skin_conditions http://en.wikipedia.org/wiki/List_of_syndromes http://en.wikipedia.org/wiki/The_Resilience_Project http://en.wikipedia.org/wiki/Fibroblast_growth_factor_receptor_2 http://en.wikipedia.org/wiki/Category:Rare_syndromes http://en.wikipedia.org/wiki/Skull_bossing http://en.wikipedia.org/wiki/Webbed_toes http://en.wikipedia.org/wiki/Category:Syndromes_with_dysmelia http://en.wikipedia.org/wiki/Dysmelia http://en.wikipedia.org/wiki/Exophthalmos http://en.wikipedia.org/wiki/Cole%E2%80%93Carpenter_syndrome http://en.wikipedia.org/wiki/Acrocephalosyndactyly http://en.wikipedia.org/wiki/Craniosynostosis http://en.wikipedia.org/wiki/List_of_congenital_disorders http://en.wikipedia.org/wiki/Chromosome_8 http://en.wikipedia.org/wiki/Category:Cell_surface_receptor_deficiencies
skos:prefLabel	Pfeiffer syndrome
skos:altLabel	Mesomelic syndrome Pfeiffer type Pfeiffer Syndrome Pfeiffer syndrome type 2 Pfeiffer type acrocephalosyndactyly
clgo:diseasesDB	32145
clgo:icd10	Q87.0
clgo:icd9	755.55
clgo:medicalCause	Genetics
clgo:meshId	D000168
clgo:omim	101600
clgo:orpha	710

About: clgr:Pfeiffer_syndrome