Global Variome shared LOVD

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

Phenotype #0000061485 Individual ID 00081841 Associated disease CWS1 Phenotype details typical mucocutaneous lesions, begnin thyroid lesions, hamartomas polys, glycogenic acanthosis, lipovascular lesions, macrocephaly (HP:0000256) Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 43y (43 years) Age/Diagnosis - Age/Onset - Phenotype/Onset 43y Protein - Owner name Michel Longy Database submission license No license selected Created by Michel Longy Date created 2016-10-28 12:16:05 +02:00 (CEST) Date last edited 2016-11-12 15:28:35 +01:00 (CET)

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