Phenotype #0000154521

Individual ID 00206651
Associated disease -
Phenotype details ocular hypertelorism, low-set ear, small mandibled, clinodacytly of the fifth finger, normokalemia, bigeminy, nonsustained VT,
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 7y
Phenotype/Onset periodic paralysis
Protein -
Owner name Ikuko Takeda
Database submission license No license selected
Created by Ikuko Takeda
Date created 2013-05-22 12:31:07 +02:00 (CEST)
Date last edited N/A

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