Phenotype #0000128936

Individual ID 00163778
Associated disease GOSHS
Phenotype details foca dermal hypoplasia (Goltz-Gorlin- oder Goltz-Syndrom)
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Gemeinschaftspraxis für Humangenetik Dresden
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-04-15 11:36:31 +02:00 (CEST)
Date last edited 2018-04-15 11:38:33 +02:00 (CEST)

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