Male infertility with azoospermia or oligozoospermia due to single gene mutation

Orpha code: 399805OMIM code: 618086

Definicja

A rare, genetic male infertility due to a sperm disorder characterized by the absence of a measurable amount of spermatozoa in the ejaculate (azoospermia), or a number of sperm in the ejaculate inferior to 15 million/mL (oligozoospermia), resulting from a mutation in a single gene known to cause azoo- or oligo-spermia. Sperm morphology may be normal.

Disease data
Klasyfikacja

Disease

Kod ORPHA
399805
Kod OMIM
618086
Kod ICD10
N46
Kod ICD11
-

No additional description.

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