Phenotype #0000115937

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00143188
Associated disease	?
Diagnosis/Initial	-
Diagnosis/Definite	-
Phenotype details	microcephaly (HP:0000252), cortical atrophy (HP:?), hypofibrinogenemia (HP:0011900)
Inheritance	Unknown
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Tumor/MSI	-
Diagnosis/Criteria	-
Owner name	Joshi Stephen
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2017-11-29 07:40:43 +01:00 (CET)
Date last edited	N/A

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