Phenotype #0000092140

Individual ID 00116692
Associated disease IFAP1
Phenotype details born with full head of hair. dry and rough skin. hypotrochosis at age 9. mild photophobia. mild myopia; IFAP syndrome; no intellectual disability
Diagnosis/Initial -
Inheritance Familial
Diagnosis/Definite -
Age/Examination 09y (9 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Emmelien Aten
Database submission license No license selected
Created by Emmelien Aten
Date created 2011-01-16 20:20:20 +01:00 (CET)
Date last edited 2017-08-08 19:45:17 +02:00 (CEST)

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