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GENATLAS PHENOTYPE

last update : 25-05-2022

Symbol	MRGH
Location	Xq27.1
Name	mental retardation, with isolated growth hormone deficiency
Corresponding gene	SOX3
Other symbol(s)	MRXS15
Main clinical features	infantile behavior, isolated growth hormone deficiency, varying degrees of mental retardation, but without other consistent phenotypic abnormalities
Genetic determination	sex linked
Function/system disorder	endocrinology
	mental retardation
Type	disease

Gene product

Name	SRY (sex determining region Y)-box 3 ?

Remark(s)