Phenotype #0000025736

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00029771
Associated disease	POF8
Phenotype details	see paper; ...; primary ovarian insufficiency with complete lack of any pubertal development and streak gonads
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Polona Le Quesne Stabej
Database submission license	No license selected
Created by	Polona Le Quesne Stabej
Date created	2015-02-08 00:21:45 +01:00 (CET)
Date last edited	2017-10-24 15:34:04 +02:00 (CEST)

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