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GENATLAS PHENOTYPE

last update : 19-03-2019

Symbol	MMAFS2
Location	6q21
Name	multiple morphological abnormalities of the flagella syndrome 2
Other name(s)	Spermatogenic failure 38
Corresponding gene	ARMC2
Other symbol(s)	MIMAF6, SPGF38
Main clinical features	primary infertility and no other clinical features, thus excluding a phenotype of primary cilia dyskinesia severe astheno-teratozoospermia due to multiple morphological anomalies of the flagella
Genetic determination	autosomal recessive
Function/system disorder	sex-genitalia
Type	disease

Remark(s)