Phenotype #0000286393

Individual ID 00393152
Associated disease PJS
Phenotype details Abnormality of skin pigmentation, Abnormal pigmentation of the oral mucosa
Diagnosis/Initial Peutz-Jeghers syndrome
Inheritance Familial, autosomal dominant
Diagnosis/Definite Peutz-Jeghers syndrome
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2021-11-26 09:43:12 +01:00 (CET)
Date last edited 2021-11-26 13:26:57 +01:00 (CET)

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