Phenotype #0000247342

Individual ID 00329152
Associated disease IP
Diagnosis/Initial incontinentia pigmenti
Diagnosis/Definite IP
Inheritance Familial, autosomal dominant
Phenotype details skin pigmentation, conical teeth, retinal detachment, alopecia, CNS problems
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 2021-02-06 13:55:30 +01:00 (CET)
Date last edited 2021-02-06 13:56:42 +01:00 (CET)

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