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References OMIM Gene GeneReviews HGMD HGNC
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
Genotype/Phenotype correlations CMO type I is an allelic disorder with phenotypic overlapping