Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 5A
Synonyms	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
ID	http://purl.bioontology.org/ontology/OMIM/164975
altLabel	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 WNT5A ONCOGENE WNT5A
cui	C0812229 C0265205
Gene Locus	3p21-p14
Gene Symbol	WNT5A
Has allelic variant	http://purl.bioontology.org/ontology/OMIM/164975.0002 http://purl.bioontology.org/ontology/OMIM/164975.0001 http://purl.bioontology.org/ontology/OMIM/164975.0003 http://purl.bioontology.org/ontology/OMIM/164975.0004
MIMTYPEMEANING	Gene with known sequence
notation	164975
OMIM Entry Type	1
OMIM MimType Value	star
prefLabel	WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 5A
tui	T028 T047

Delete	Subject	Author	Type	Created
No notes to display

Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/ICD10CM/Q87.1	International Classification of Diseases, Version 10 - Clinical Modification	CUI
	http://purl.bioontology.org/ontology/MESH/C562492	Medical Subject Headings	CUI