Phenotype #0000066705

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00087124
Associated disease	PRLTS
Phenotype details	see paper;, ..., profound deafness, amenorrhea II (onset 25y), no neurological symptoms, hypothyroidism
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	<03y
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2016-11-13 16:06:45 +01:00 (CET)
Date last edited	N/A

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