Phenotype #0000061486

Individual ID 00081842
Associated disease CWS1
Phenotype details Typical mucocutaneous lesions, begnin thyroid lesions,begnin breast lesions,hamartomas polyps,glycogenic acanthosis, lipovascular lesions, macrocephaly, uterine fibromas
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 62y (62 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset 62y
Protein -
Owner name Michel Longy
Database submission license No license selected
Created by Michel Longy
Date created 2016-10-28 13:57:29 +02:00 (CEST)
Date last edited 2016-11-12 15:34:07 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.