Phenotype #0000144218

Individual ID 00183513
Associated disease OPMD
Phenotype details more sever phenotype
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite OPMD
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-01-16 11:38:09 +01:00 (CET)
Date last edited 2012-03-09 20:07:18 +01:00 (CET)

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