Global Variome shared LOVD

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

Phenotype #0000154581 Individual ID 00206711 Associated disease - Phenotype details hypertelorism, micrognathia,Clinodactyly, a broad-based nose, low-set ears, CMAP decrease, normokalemia, asymptomatic premature ventricular, weakness was 2–3 days Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis 16y Age/Onset 11y 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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