Phenotype #0000092162

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00116642
Associated disease	IFAP1
Phenotype details	Single patch of alopecia; normal skin apart from eczema during childhood); normal eyes (apart from surgically-corrected strabismus); IFAP syndrome
Diagnosis/Initial	-
Inheritance	Familial, X-linked dominant, male sparing
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Karl-Heinz Grzeschik
Database submission license	No license selected
Created by	Karl-Heinz Grzeschik
Date created	2012-11-27 12:28:06 +01:00 (CET)
Date last edited	N/A

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