Hypochondroplasia - CaLiGraph

CaLiGraph

Property	Value
rdf:type	owl:NamedIndividual Autosomal dominant disorder Rare disease Cell surface receptor deficiency Growth disorder
rdfs:label	Hypochondroplasia
owl:sameAs	dbr:Hypochondroplasia
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Autosomal_dominant_disorders http://en.wikipedia.org/wiki/Category:Rare_diseases http://en.wikipedia.org/wiki/List_of_diseases_(H) http://en.wikipedia.org/wiki/Macrocephaly http://en.wikipedia.org/wiki/Category:Growth_disorders http://en.wikipedia.org/wiki/Category:Cell_surface_receptor_deficiencies http://en.wikipedia.org/wiki/Chromosome_4
skos:prefLabel	Hypochondroplasia
skos:altLabel	hypochondroplasia
clgo:diseasesDB	32832
clgo:geneReviewsId	NBK1477
clgo:geneReviewsName	Hypochondroplasia
clgo:icd10	Q77.4
clgo:omim	146000
clgo:symptom	Osteochondrodysplasia
clgo:treatment	Laminectomy
is clgo:differentialDiagnosis of	Achondroplasia

About: clgr:Hypochondroplasia