Global Variome shared LOVD

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Phenotype #0000226758 Individual ID 00299448 Associated disease INFM Phenotype details see paper; ..., azoospermia (3/4), oligozoospermia (1/4) Diagnosis/Initial reduced sperm levels Inheritance Familial, autosomal recessive Diagnosis/Definite SPGF14 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2020-04-16 12:10:42 +02:00 (CEST) Date last edited N/A

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