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GENATLAS PHENOTYPE

last update : 14/12/06

Symbol	CMO2
Location	8q24.3
Name	corticosterone methyloxydase type II deficiency
Other name(s)	aldosterone deficiency due to defect in 18-hydroxylase
Corresponding gene	CYP11B2
Other symbol(s)	FHHA2, CMO-II
Main clinical features	salt losing syndrome
Genetic determination	autosomal recessive
Related entries	CMO1
Function/system disorder	endocrinology
Type	disease

Remark(s)

Genotype/Phenotype correlations

CMO type I is an allelic disorder with phenotypic overlapping