Phenotype #0000247363

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00001467
Associated disease	IP
Diagnosis/Initial	incontinentia pigmenti
Diagnosis/Definite	IP
Inheritance	Familial, X-linked recessive
Phenotype details	see paper; ..., incontinentia pigmenti, osteopetrosis, lymphedema, ectodermal dysplasia, immune deficiency
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2021-02-07 11:56:49 +01:00 (CET)
Date last edited	2021-02-07 14:44:37 +01:00 (CET)

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