Global Variome shared LOVD

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Phenotype #0000024758 Individual ID 00028731 Associated disease FMD1 Phenotype details supraorbital ridging,hypertelorism, broad nasal bridge, small chin, irregular teeth,and long slender fingers with 3ñ5 camptodactyly Diagnosis/Initial - Inheritance Familial Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Yu Sun Database submission license No license selected Created by Yu Sun Date created 2010-04-02 16:29:25 +02:00 (CEST) Date last edited N/A

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