Phenotype #0000162016

Individual ID 00213562
Associated disease CMYO4A;CFTD
Phenotype details -
Diagnosis/Initial congenital fibre type disproportion
Inheritance Familial, autosomal dominant
Diagnosis/Definite CFTD
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 2008-09-22 10:14:28 +02:00 (CEST)
Date last edited 2012-03-18 13:26:42 +01:00 (CET)

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