Phenotype #0000001832

Individual ID 00002920
Associated disease CMYO6;MYPOP
Phenotype details pronounced opthalmoplegia; no ptosis; ...
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 42y (42 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Homa Tajsharghi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-09-19 19:25:22 +02:00 (CEST)
Date last edited N/A

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