Laron syndrome - CaLiGraph

CaLiGraph

Property	Value
rdf:type	owl:NamedIndividual Eponymous disease Rare syndrome Syndrome affecting stature Growth hormone Autosomal recessive disorder Cause of hypoglycemia Disorder causing seizures MeSH code (C16) Cell surface receptor deficiency MeSH code (C05)
rdfs:label	Laron syndrome
owl:sameAs	dbr:Laron_syndrome
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Growth_hormones http://en.wikipedia.org/wiki/List_of_diseases_(L) http://en.wikipedia.org/wiki/List_of_eponymous_diseases http://en.wikipedia.org/wiki/List_of_syndromes http://en.wikipedia.org/wiki/Category:Rare_syndromes http://en.wikipedia.org/wiki/Category:Syndromes_affecting_stature http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16) http://en.wikipedia.org/wiki/List_of_causes_of_hypoglycemia http://en.wikipedia.org/wiki/Category:Autosomal_recessive_disorders http://en.wikipedia.org/wiki/Category:Disorders_causing_seizures http://en.wikipedia.org/wiki/Category:Cell_surface_receptor_deficiencies http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C05)
skos:prefLabel	Laron syndrome
skos:altLabel	Laron dwarfism Laron-type dwarfism Primary IGFD laron syndrome
clgo:differentialDiagnosis	Hypopituitarism STAT5B
clgo:diseasesDB	7262
clgo:eMedicineSubject	ped
clgo:eMedicineTopic	1277
clgo:icd10	E34.3
clgo:icd9	259.4
clgo:medicalCause	Autosome
clgo:meshId	D046150
clgo:omim	262500
clgo:orpha	633
clgo:symptom	Dwarfism
clgo:treatment	Insulin-like growth factor 1 Mecasermin
clgo:medicalSpecialty	Endocrinology Medical genetics Pediatrics
is clgo:knownFor of	Zvi Laron

About: clgr:Laron_syndrome