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 International |
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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