Phenotype #0000025778

Individual ID 00029825
Associated disease RIEG1
Phenotype details camptodactyly of the right fifth finger, clinodactyly of the left one, bilateral Simian creases,atrial and ventricular septal defects,omphalocele
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Moretza Seifi
Database submission license No license selected
Created by Moretza Seifi
Date created 2015-02-12 04:36:12 +01:00 (CET)
Date last edited 2015-02-20 14:12:38 +01:00 (CET)

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