Ellis–Van Creveld syndrome

Human disease

Wikidata entity: Q1332448

Wikimedia Commons category is Ellis–van Creveld syndrome

P373 Commons category String Ellis–van Creveld syndrome ???
P2888 exact match Url Ontology Lookup Service (OLS) ???
P2888 exact match Url Disease Ontology - Institute for Genome Sciences @ University of Maryland ???
P2888 exact match Url Ontology Lookup Service (OLS) ???
P2293 genetic association ... Q17917650 (EVC) EVC
P2293 genetic association ... Q18040462 (DYNC2LI1) DYNC2LI1
P2293 genetic association ... Q18050450 (EVC2) EVC2
P1995 health specialty ... Q1071953 (medical genetics) medical genetics
P1692 ICD-9-CM String 756.55 ???
P31 instance of ... Q112193867 (class of disease) class of disease
P31 instance of ... Q55788864 (developmental defect during embryogenesis) developmental defect during embryogenesis
P138 named after ... Q667397 (Richard Ellis) Richard Ellis
P138 named after ... Q2287939 (Simon van Creveld) Simon van Creveld
P1748 NCI Thesaurus ID String C84684 ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P279 subclass of ... Q12136 (disease) disease
P279 subclass of ... Q179630 (syndrome) syndrome
P279 subclass of ... Q10267817 (autosomal recessive disease) autosomal recessive disease
P279 subclass of ... Q55785518 (rare syndrome with cardiac malformations) rare syndrome with cardiac malformations
P279 subclass of ... Q55785601 (rare abdominal surgical disease) rare abdominal surgical disease
P279 subclass of ... Q55788832 (syndromic renal or urinary tract malformation) syndromic renal or urinary tract malformation
External Ids
P699Disease Ontology IDDOID:12714
P557DiseasesDB29309
P673eMedicine ID943684
P1417Encyclopædia Britannica Online IDscience/chondroectodermal-dysplasia
P646Freebase ID/m/0525gt
P4317GARD rare disease ID1301
P668GeneReviews IDNBK596643
P7464Genetics Home Reference Conditions IDellis-van-creveld-syndrome
P4229ICD-10-CMQ77.6
P7807ICD-11 ID (Foundation)278346811
P665KEGG IDH00503
P604MedlinePlus ID001667
P604MedlinePlus ID001667
P486MeSH descriptor IDD004613
P672MeSH tree codeC05.116.099.708.327
P672MeSH tree codeC16.131.077.350.398
P672MeSH tree codeC16.131.831.350.398
P672MeSH tree codeC16.320.850.250.398
P672MeSH tree codeC17.800.804.350.398
P672MeSH tree codeC17.800.827.250.398
P6366Microsoft Academic ID (discontinued)2776199626
P5270Mondo IDMONDO_0009162
P492OMIM ID225500
P492OMIM ID225500
P1550Orphanet ID289
P4233PatientsLikeMe condition IDellis-van-creveld-syndrome
P2892UMLS CUIC0013903
P11430UniProt disease IDDI-00449

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