Phenotype #0000119186

Individual ID 00146446
Associated disease MEAX
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details -
Inheritance Familial, X-linked recessive
Age/Examination -
Age/Onset -
Phenotype/Onset -
Protein IHC VMA21 reduced
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 2010-03-12 16:21:08 +01:00 (CET)
Date last edited 2012-03-04 15:57:59 +01:00 (CET)

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