Disease #00882 (cancer, esophageal, OMIM:133239)

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Official abbreviation	-
Name	cancer, esophageal
OMIM ID	133239
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 7 genes	DCC, DEC1, DLEC1, LZTS1, RNF6, TGFBR2, WWOX
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A