Phenotype #0000036649
Individual ID |
00049867 |
Associated disease |
RTS2 |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Initial |
- |
Age/Examination |
02y (2 years) |
Diagnosis/Definite |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Phenotype details |
poikiloderma, microdontia, abnormalities of the long bones, short stature, delayed motor development, nutritional problems, osteosarcoma |
Protein |
- |
Owner name |
Sabina Gallati, Prof. |
Database submission license |
No license selected |
Created by |
Sabina Gallati, Prof. |
Date created |
2015-09-13 16:39:06 +02:00 (CEST) |
Date last edited |
2016-01-26 02:58:19 +01:00 (CET) |
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