Phenotype #0000106801

Individual ID 00133223
Associated disease INFM
Phenotype details male infertility (HP:0003251), oligospermia (HP:0000798), asthenospermia (HP:0012207)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite SPGF70
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Yeşerin Yıldırım
Database submission license No license selected
Created by Yeşerin Yıldırım
Date created 2017-11-23 12:10:35 +01:00 (CET)
Date last edited 2022-04-08 19:44:51 +02:00 (CEST)

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