Phenotype #0000228654

Individual ID 00301523
Associated disease RMD2;LGMD1C
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Helen Latsoudis
Database submission license No license selected
Created by Helen Latsoudis
Date created 2020-05-18 15:36:04 +02:00 (CEST)
Date last edited 2020-05-18 15:56:20 +02:00 (CEST)

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