Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/615706 http://purl.bioontology.org/ontology/OMIM/615706
Preferred Name	AURICULOCONDYLAR SYNDROME 3
Synonyms	ARCND3
Type	http://www.w3.org/2002/07/owl#Class

altLabel	ARCND3
prefLabel	AURICULOCONDYLAR SYNDROME 3
Gene Symbol	ARCND3 EDN1 QME
Scope Statement	Caused by mutation in the endothelin-1 gene (EDN1, 131240.0002) [MOLECULAR BASIS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU001174 http://purl.bioontology.org/ontology/OMIM/MTHU000576 http://purl.bioontology.org/ontology/OMIM/MTHU069803 http://purl.bioontology.org/ontology/OMIM/MTHU069804 http://purl.bioontology.org/ontology/OMIM/MTHU044993 http://purl.bioontology.org/ontology/OMIM/MTHU043141 http://purl.bioontology.org/ontology/OMIM/MTHU007653 http://purl.bioontology.org/ontology/OMIM/MTHU001172 http://purl.bioontology.org/ontology/OMIM/MTHU036550 http://purl.bioontology.org/ontology/OMIM/MTHU036924 http://purl.bioontology.org/ontology/OMIM/MTHU017700 http://purl.bioontology.org/ontology/OMIM/MTHU069802 http://purl.bioontology.org/ontology/OMIM/MTHU044995 http://purl.bioontology.org/ontology/OMIM/MTHU044996 http://purl.bioontology.org/ontology/OMIM/MTHU044994 http://purl.bioontology.org/ontology/OMIM/MTHU005783 See more See less
tui	T047
Gene Locus	6p24-p23
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	615706
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000016
cui	C3810332
OMIM Entry Type	3
OMIM MimType Value	pound

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