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GENATLAS PHENOTYPE

last update : 11-10-2022

Symbol	KAL9
Location	4q27
Name	Kallmann syndrome 9
Other name(s)	hypogonadotropic hypogonadism 25 with anosmia
Corresponding gene	NDNF
Other symbol(s)	HH25
Main clinical features	hypogonadotropic hypogonadism, characterized by infertility and the absence of puberty severe GNRH deficiency and anosmia, cryptorchidism and micropenis,
Genetic determination	autosomal dominant
Function/system disorder	sex-genitalia
	endocrinology
Type	disease

Remark(s)