Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000174335 Individual ID 00233913 Associated disease FDH Phenotype details nail dysplasia (HP:0002164), skin hypoplasia (HP:0008065); Diagnosis/Initial Goltz-Gorlin syndrome Inheritance Isolated (sporadic) Diagnosis/Definite FDH Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Maria Paola Lombardi Database submission license No license selected Created by Maria Paola Lombardi Date created 2010-03-18 15:03:45 +01:00 (CET) Date last edited 2010-03-31 11:52:41 +02:00 (CEST)

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