Prader–Willi syndrome

Property	Value
rdf:type	owl:NamedIndividual Eponymous disease Intersex variation Neurological condition or disorder Rare genetic syndrome Skin condition Genodermatose Syndrome with obesity Autosomal monosomy or deletion Genetic anomaly Congenital disorder ICD-9 codes 740–759: congenital anomaly MeSH code (C10) MeSH code (C16) MeSH code (C18) Genetic disorder
rdfs:label	Prader–Willi syndrome
owl:sameAs	dbr:Prader–Willi_syndrome
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Congenital_disorders http://en.wikipedia.org/wiki/Category:Syndromes_with_obesity http://en.wikipedia.org/wiki/Micrognathism http://en.wikipedia.org/wiki/Category:Genodermatoses http://en.wikipedia.org/wiki/Karyotype http://en.wikipedia.org/wiki/Polyphagia http://en.wikipedia.org/wiki/Category:Autosomal_monosomies_and_deletions http://en.wikipedia.org/wiki/Category:Genetic_anomalies http://en.wikipedia.org/wiki/Category:Intersex_variations http://en.wikipedia.org/wiki/Category:Rare_genetic_syndromes http://en.wikipedia.org/wiki/List_of_diseases_(P) http://en.wikipedia.org/wiki/List_of_eponymous_diseases http://en.wikipedia.org/wiki/List_of_neurological_conditions_and_disorders http://en.wikipedia.org/wiki/List_of_skin_conditions http://en.wikipedia.org/wiki/List_of_syndromes http://en.wikipedia.org/wiki/List_of_genetic_disorders http://en.wikipedia.org/wiki/Gonadotropin-releasing_hormone_insensitivity http://en.wikipedia.org/wiki/Childhood_obesity http://en.wikipedia.org/wiki/Epigenetics_of_human_development http://en.wikipedia.org/wiki/Uniparental_disomy http://en.wikipedia.org/wiki/Andrea_Prader http://en.wikipedia.org/wiki/Angelman_syndrome http://en.wikipedia.org/wiki/Microdeletion_syndrome http://en.wikipedia.org/wiki/Breech_birth http://en.wikipedia.org/wiki/Growth_hormone_therapy http://en.wikipedia.org/wiki/Eating_disorder http://en.wikipedia.org/wiki/List_of_ICD-9_codes_740%E2%80%93759:_congenital_anomalies 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/List_of_MeSH_codes_(C18) http://en.wikipedia.org/wiki/Hypotonia http://en.wikipedia.org/wiki/Growth_hormone_deficiency
skos:prefLabel	Prader–Willi syndrome
skos:altLabel	Prader Willi Prader–Willi syndrome Prader-Labhart-Willi Prader-Willi Prader-Willi Syndrome Prader-Willi syndrome Prader–Willi Prader–Willi Syndrome Prader–Willi_syndrome Prata–Liberal–Goncalves syndrome prader-willi syndrome
clgo:diseasesDB	10481
clgo:eMedicineSubject	ped
clgo:eMedicineTopic	1880
clgo:geneReviewsId	NBK1330
clgo:geneReviewsName	Prader-Willi syndrome
clgo:icd10	Q87.1
clgo:icd9	759.81
clgo:medicalCause	Genetic disorder
clgo:medicalDiagnosis	Genetic testing
clgo:medication	Growth hormone therapy
clgo:medlinePlus	001605
clgo:meshId	D011218
clgo:omim	176270
clgo:orpha	739
clgo:symptom	Hypotonia Developmental disability
clgo:treatment	Behaviour therapy
is clgo:differentialDiagnosis of	1p36 deletion syndrome Growth hormone deficiency Spinal muscular atrophy Angelman syndrome Snyder–Robinson syndrome
is clgo:knownFor of	Andrea Prader
is clgo:medicalCause of	Abdominal obesity

About: clgr:Prader–Willi_syndrome