Phenotype #0000161579

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00213098
Associated disease	?
Diagnosis/Initial	developmental syndrome
Diagnosis/Definite	-
Phenotype details	growth retardation, microcephaly, no hypotonia, upslanting palpebral fissures, bifid flat nasal tip, foot ray anomaly (short fourth ray on the right foot); 11d-died from massive thrombosis
Inheritance	Familial, autosomal dominant
Age/Examination	00y00m11d (11 days)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Tumor/MSI	-
Diagnosis/Criteria	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2019-01-09 19:48:16 +01:00 (CET)
Date last edited	N/A

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