Phenotype #0000237090

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00311842
Associated disease	RRS
Phenotype details	severe brachydactyly (BDB1); patient BDB_005 has deletion of the same region
Diagnosis/Initial	Robinow syndrome
Inheritance	-
Diagnosis/Definite	RRS1
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Jacopo Celli
Database submission license
Created by	Jacopo Celli
Date created	2010-04-28 12:53:12 +02:00 (CEST)
Date last edited	2010-04-29 08:54:58 +02:00 (CEST)

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