Snyder–Robinson syndrome

CaLiGraph

Property	Value
rdf:type	owl:NamedIndividual Rare syndrome Congenital disorder ICD-9 codes 740–759: congenital anomaly
rdfs:label	Snyder–Robinson syndrome
owl:sameAs	dbr:Snyder–Robinson_syndrome
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Congenital_disorders http://en.wikipedia.org/wiki/Marfanoid http://en.wikipedia.org/wiki/Category:Rare_syndromes http://en.wikipedia.org/wiki/List_of_ICD-9_codes_740%E2%80%93759:_congenital_anomalies http://en.wikipedia.org/wiki/List_of_congenital_disorders http://en.wikipedia.org/wiki/Hypotonia
skos:prefLabel	Snyder–Robinson syndrome
clgo:gradNum	5615
clgo:differentialDiagnosis	Prader–Willi syndrome Cerebral palsy Urban–Rogers–Meyer syndrome Rett syndrome Glycerol kinase
clgo:diseasesDB	35186
clgo:geneReviewsId	NBK144284
clgo:icd10	Q87.8
clgo:medicalCause	Genetics
clgo:omim	309583
clgo:orpha	3063
clgo:symptom	Osteoporosis Facial symmetry Hypotonia Intellectual disability Kyphoscoliosis

About: clgr:Snyder–Robinson_syndrome