Individual ID |
00208593 |
Associated disease |
CLP |
Phenotype details |
minor anomalies in some affected patients in this family: hypodontia, dry skin, duplicated thumb |
Diagnosis/Initial |
- |
Inheritance |
Familial, autosomal dominant |
Diagnosis/Definite |
- |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
congenital |
Protein |
- |
Owner name |
J.H.L.M. (Hans) van Bokhoven |
Database submission license |
No license selected |
Created by |
J.H.L.M. (Hans) van Bokhoven |
Date created |
2018-12-11 13:35:20 +01:00 (CET) |
Date last edited |
2018-12-13 15:01:00 +01:00 (CET) |