Disease #00212 (SCZD (schizophrenia (SCZD)), OMIM:181500)

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Official abbreviation	SCZD
Name	schizophrenia (SCZD)
OMIM ID	181500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 14 genes	AKT1, APOL2, APOL4, CHI3L1, COMT, DAO, DAOA, DISC1, DISC2, DRD3, DTNBP1, HTR2A, MTHFR, RTN4R
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-09-24 21:08:12 +02:00 (CEST)
Date last edited	N/A