Phenotype #0000073818

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00095419
Associated disease	DD
Phenotype details	Hypotonia, microcephaly, speech delay, renal disease (hypomagnesemia)
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	00y00m03d
Phenotype/Onset	-
Protein	-
Owner name	Asaf Ta-Shma
Database submission license	No license selected
Created by	Asaf Ta-Shma
Date created	2017-01-16 11:41:19 +01:00 (CET)
Date last edited	2017-01-17 16:52:05 +01:00 (CET)

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