Online Mendelian Inheritance in Man - CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY - Classes | NCBO OntoPortal Appliance

Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Details
Visualization
Notes ( 0 )
Class Mappings ( )

Preferred Name	CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY
Synonyms	CCF
ID	http://purl.bioontology.org/ontology/OMIM/119800
altLabel	CCF
cui	C0009081
Gene Locus	5q31
Gene Symbol	PITX1 LBNBG POTX BFT CCF PTX1
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU036592 http://purl.bioontology.org/ontology/OMIM/MTHU036595 http://purl.bioontology.org/ontology/OMIM/MTHU036590 http://purl.bioontology.org/ontology/OMIM/MTHU001112 http://purl.bioontology.org/ontology/OMIM/MTHU036596 http://purl.bioontology.org/ontology/OMIM/MTHU036594 http://purl.bioontology.org/ontology/OMIM/MTHU036591 http://purl.bioontology.org/ontology/OMIM/MTHU036593 http://purl.bioontology.org/ontology/OMIM/MTHU036589
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	119800
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY
tui	T019

Subscribe to notes emails

Delete	Subject	Author	Type	Created
No notes to display

Create New Mapping

Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/ICD10/Q66.0	International Classification of Diseases, Version 10	CUI
	http://purl.bmicc.cn/ontology/ICD10CN/Q66.0	International Classification of Diseases, 10th Edition, China	CUI
	http://purl.bioontology.org/ontology/ICD10CM/Q66.0	International Classification of Diseases, Version 10 - Clinical Modification	CUI
	http://purl.bioontology.org/ontology/ICD10CM/Q66.89	International Classification of Diseases, Version 10 - Clinical Modification	CUI
	http://purl.bioontology.org/ontology/MESH/D003025	Medical Subject Headings	CUI