Phenotype #0000084252

Individual ID 00106448
Associated disease MYOP
Phenotype details myopathy, congenital
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Tom Winder
Database submission license No license selected
Created by Tom Winder
Date created 2011-10-04 17:29:56 +02:00 (CEST)
Date last edited 2012-03-09 19:12:55 +01:00 (CET)

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